Picolinamide compounds with fungicidal activity

ABSTRACT

This disclosure relates to picolinamides of Formula I and their use as fungicides.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 15/036,314 filed May 12, 2016, which is a U.S. National Phase Patent Application based on International Application No. PCT/US2015/066760 filed Dec. 18, 2015, which claims the benefit of U.S. Provisional Patent Application Ser. Nos. 62/098,120 filed Dec. 30, 2014 and 62/098,122 filed Dec. 30, 2014, which are expressly incorporated by reference herein.

BACKGROUND & SUMMARY

Fungicides are compounds, of natural or synthetic origin, which act to protect and/or cure plants against damage caused by agriculturally relevant fungi. Generally, no single fungicide is useful in all situations. Consequently, research is ongoing to produce fungicides that may have better performance, are easier to use, and cost less.

The present disclosure relates to picolinamides and their use as fungicides. The compounds of the present disclosure may offer protection against ascomycetes, basidiomycetes, deuteromycetes and oomycetes.

One embodiment of the present disclosure may include compounds of Formula I:

in which: X is hydrogen or C(O)R₅;

Y is hydrogen, C(O)R₅, or Q;

Q is

wherein: Z is N or CH;

R₁ is hydrogen or alkyl, each optionally substituted with 0, 1 or multiple R₈;

R₂ is methyl;

R₃ is chosen from aryl or heteroaryl, each optionally substituted with 0, 1 or multiple R₈;

R₄ is chosen from hydrogen, halo, hydroxyl, alkyl or alkoxy;

R₅ is chosen from alkoxy or benzyloxy, each optionally substituted with 0, 1, or multiple R₈;

R₆ is chosen from hydrogen, alkoxy, or halo, each optionally substituted with 0, 1, or multiple R₈;

R₇ is chosen from hydrogen, —C(O)R₉, or —CH₂OC(O)R₉;

R₈ is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, alkynyl, alkoxy, cyano or heterocyclyl, each optionally substituted with 0, 1, or multiple R₁₀:

R₉ is chosen from alkyl, alkoxy, or aryl, each optionally substituted with 0, 1, or multiple R₈;

R₁₀ is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, alkoxy, or heterocyclyl;

R₁₁ is chosen from hydrogen or alkyl, substituted with 0, 1, or multiple R₈;

R₁₂ is chosen from aryl or heteroaryl, each optionally substituted with 0, 1 or multiple R₈.

Another embodiment of the present disclosure may include a fungicidal composition for the control or prevention of fungal attack comprising the compounds described above and a phytologically acceptable carrier material.

Yet another embodiment of the present disclosure may include a method for the control or prevention of fungal attack on a plant, the method including the steps of applying a fungicidally effective amount of one or more of the compounds described above to at least one of the fungus, the plant, and an area adjacent to the plant.

It will be understood by those skilled in the art that the following terms may include generic “R”-groups within their definitions, e.g., “the term alkoxy refers to an —OR substituent”. It is also understood that within the definitions for the following terms, these “R” groups are included for illustration purposes and should not be construed as limiting or being limited by substitutions about Formula I.

The term “alkyl” refers to a branched, unbranched, or saturated cyclic carbon chain, including, but not limited to, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, tertiary butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.

The term “alkenyl” refers to a branched, unbranched or cyclic carbon chain containing one or more double bonds including, but not limited to, ethenyl, propenyl, butenyl, isopropenyl, isobutenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, and the like.

The term “alkynyl” refers to a branched or unbranched carbon chain containing one or more triple bonds including, but not limited to, propynyl, butynyl, and the like.

The terms “aryl” and “Ar” refer to any aromatic ring, mono- or bi-cyclic, containing 0 heteroatoms.

The term “heterocyclyl” refers to any aromatic or non-aromatic ring, mono- or bi-cyclic, containing one or more heteroatoms.

The term “alkoxy” refers to an —OR substituent.

The term “acyloxy” refers to an —OC(O)R substituent.

The term “cyano” refers to a —C≡N substituent.

The term “hydroxyl” refers to an —OH substituent.

The term “amino” refers to a —N(R)₂ substituent.

The term “arylalkoxy” refers to —O(CH₂)_(n)Ar where n is an integer selected from the list 1, 2, 3, 4, 5, or 6.

The term “haloalkoxy” refers to an —OR—X substituent, wherein X is Cl, F, Br, or I, or any combination thereof.

The term “haloalkyl” refers to an alkyl, which is substituted with Cl, F, I, or Br or any combination thereof.

The term “halogen” or “halo” refers to one or more halogen atoms, defined as F, Cl, Br, and I.

The term “nitro” refers to a —NO₂ substituent.

The term thioalkyl refers to an —SR substituent.

Throughout the disclosure, reference to the compounds of Formula I is read as also including all stereoisomers, for example diastereomers, enantiomers, and mixtures thereof. In another embodiment, Formula I is read as also including salts or hydrates thereof. Exemplary salts include, but are not limited to: hydrochloride, hydrobromide, hydroiodide, trifluoroacetate, and trifluoromethane sulfonate.

It is also understood by those skilled in the art that additional substitution is allowable, unless otherwise noted, as long as the rules of chemical bonding and strain energy are satisfied and the product still exhibits fungicidal activity.

Another embodiment of the present disclosure is a use of a compound of Formula I, for protection of a plant against attack by a phytopathogenic organism or the treatment of a plant infested by a phytopathogenic organism, comprising the application of a compound of Formula I, or a composition comprising the compound to soil, a plant, a part of a plant, foliage, and/or roots.

Additionally, another embodiment of the present disclosure is a composition useful for protecting a plant against attack by a phytopathogenic organism and/or treatment of a plant infested by a phytopathogenic organism comprising a compound of Formula I and a phytologically acceptable carrier material.

DETAILED DESCRIPTION

The compounds of the present disclosure may be applied by any of a variety of known techniques, either as the compounds or as formulations comprising the compounds. For example, the compounds may be applied to the roots or foliage of plants for the control of various fungi, without damaging the commercial value of the plants. The materials may be applied in the form of any of the generally used formulation types, for example, as solutions, dusts, wettable powders, flowable concentrate, or emulsifiable concentrates.

Preferably, the compounds of the present disclosure are applied in the form of a formulation, comprising one or more of the compounds of Formula I with a phytologically acceptable carrier. Concentrated formulations may be dispersed in water, or other liquids, for application, or formulations may be dust-like or granular, which may then be applied without further treatment. The formulations can be prepared according to procedures that are conventional in the agricultural chemical art.

The present disclosure contemplates all vehicles by which one or more of the compounds may be formulated for delivery and use as a fungicide. Typically, formulations are applied as aqueous suspensions or emulsions. Such suspensions or emulsions may be produced from water-soluble, water-suspendible, or emulsifiable formulations which are solids, usually known as wettable powders; or liquids, usually known as emulsifiable concentrates, aqueous suspensions, or suspension concentrates. As will be readily appreciated, any material to which these compounds may be added may be used, provided it yields the desired utility without significant interference with the activity of these compounds as antifungal agents.

Wettable powders, which may be compacted to form water-dispersible granules, comprise an intimate mixture of one or more of the compounds of Formula I, an inert carrier and surfactants. The concentration of the compound in the wettable powder may be from about 10 percent to about 90 percent by weight based on the total weight of the wettable powder, more preferably about 25 weight percent to about 75 weight percent. In the preparation of wettable powder formulations, the compounds may be compounded with any finely divided solid, such as prophyllite, talc, chalk, gypsum, Fuller's earth, bentonite, attapulgite, starch, casein, gluten, montmorillonite clays, diatomaceous earths, purified silicates or the like. In such operations, the finely divided carrier and surfactants are typically blended with the compound(s) and milled.

Emulsifiable concentrates of the compounds of Formula I may comprise a convenient concentration, such as from about 1 weight percent to about 50 weight percent of the compound, in a suitable liquid, based on the total weight of the concentrate. The compounds may be dissolved in an inert carrier, which is either a water-miscible solvent or a mixture of water-immiscible organic solvents, and emulsifiers. The concentrates may be diluted with water and oil to form spray mixtures in the form of oil-in-water emulsions. Useful organic solvents include aromatics, especially the high-boiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha. Other organic solvents may also be used, for example, terpenic solvents, including rosin derivatives, aliphatic ketones, such as cyclohexanone, and complex alcohols, such as 2-ethoxyethanol.

Emulsifiers which may be advantageously employed herein may be readily determined by those skilled in the art and include various nonionic, anionic, cationic and amphoteric emulsifiers, or a blend of two or more emulsifiers. Examples of nonionic emulsifiers useful in preparing the emulsifiable concentrates include the polyalkylene glycol ethers and condensation products of alkyl and aryl phenols, aliphatic alcohols, aliphatic amines or fatty acids with ethylene oxide, propylene oxides such as the ethoxylated alkyl phenols and carboxylic esters solubilized with the polyol or polyoxyalkylene. Cationic emulsifiers include quaternary ammonium compounds and fatty amine salts. Anionic emulsifiers include the oil-soluble salts (e.g., calcium) of alkylaryl sulfonic acids, oil-soluble salts or sulfated polyglycol ethers and appropriate salts of phosphated polyglycol ether.

Representative organic liquids which may be employed in preparing the emulsifiable concentrates of the compounds of the present disclosure are the aromatic liquids such as xylene, propyl benzene fractions; or mixed naphthalene fractions, mineral oils, substituted aromatic organic liquids such as dioctyl phthalate; kerosene; dialkyl amides of various fatty acids, particularly the dimethyl amides of fatty glycols and glycol derivatives such as the n-butyl ether, ethyl ether or methyl ether of diethylene glycol, the methyl ether of triethylene glycol, petroleum fractions or hydrocarbons such as mineral oil, aromatic solvents, paraffinic oils, and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable oils; and the like. Mixtures of two or more organic liquids may also be employed in the preparation of the emulsifiable concentrate. Organic liquids include xylene, and propyl benzene fractions, with xylene being most preferred in some cases. Surface-active dispersing agents are typically employed in liquid formulations and in an amount of from 0.1 to 20 percent by weight based on the combined weight of the dispersing agent with one or more of the compounds. The formulations can also contain other compatible additives, for example, plant growth regulators and other biologically active compounds used in agriculture.

Aqueous suspensions comprise suspensions of one or more water-insoluble compounds of Formula I, dispersed in an aqueous vehicle at a concentration in the range from about 1 to about 50 weight percent, based on the total weight of the aqueous suspension. Suspensions are prepared by finely grinding one or more of the compounds, and vigorously mixing the ground material into a vehicle comprised of water and surfactants chosen from the same types discussed above. Other components, such as inorganic salts and synthetic or natural gums, may also be added to increase the density and viscosity of the aqueous vehicle.

The compounds of Formula I can also be applied as granular formulations, which are particularly useful for applications to the soil. Granular formulations generally contain from about 0.5 to about 10 weight percent, based on the total weight of the granular formulation of the compound(s), dispersed in an inert carrier which consists entirely or in large part of coarsely divided inert material such as attapulgite, bentonite, diatomite, clay or a similar inexpensive substance. Such formulations are usually prepared by dissolving the compounds in a suitable solvent and applying it to a granular carrier which has been preformed to the appropriate particle size, in the range of from about 0.5 to about 3 mm. A suitable solvent is a solvent in which the compound is substantially or completely soluble. Such formulations may also be prepared by making a dough or paste of the carrier and the compound and solvent, and crushing and drying to obtain the desired granular particle.

Dusts containing the compounds of Formula I may be prepared by intimately mixing one or more of the compounds in powdered form with a suitable dusty agricultural carrier, such as, for example, kaolin clay, ground volcanic rock, and the like. Dusts can suitably contain from about 1 to about 10 weight percent of the compounds, based on the total weight of the dust.

The formulations may additionally contain adjuvant surfactants to enhance deposition, wetting, and penetration of the compounds onto the target crop and organism. These adjuvant surfactants may optionally be employed as a component of the formulation or as a tank mix. The amount of adjuvant surfactant will typically vary from 0.01 to 1.0 percent by volume, based on a spray-volume of water, preferably 0.05 to 0.5 volume percent. Suitable adjuvant surfactants include, but are not limited to ethoxylated nonyl phenols, ethoxylated synthetic or natural alcohols, salts of the esters or sulfosuccinic acids, ethoxylated organosilicones, ethoxylated fatty amines, blends of surfactants with mineral or vegetable oils, crop oil concentrate (mineral oil (85%)+emulsifiers (15%)); nonylphenol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C₉-C₁₁ alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (C₁₂-C₁₆) ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate+urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG(400) dioleate-99. The formulations may also include oil-in-water emulsions such as those disclosed in U.S. patent application Ser. No. 11/495,228, the disclosure of which is expressly incorporated by reference herein.

The formulations may optionally include combinations that contain other pesticidal compounds. Such additional pesticidal compounds may be fungicides, insecticides, herbicides, nematocides, miticides, arthropodicides, bactericides or combinations thereof that are compatible with the compounds of the present disclosure in the medium selected for application, and not antagonistic to the activity of the present compounds. Accordingly, in such embodiments, the other pesticidal compound is employed as a supplemental toxicant for the same or for a different pesticidal use. The compounds of Formula I and the pesticidal compound in the combination can generally be present in a weight ratio of from 1:100 to 100:1.

The compounds of the present disclosure may also be combined with other fungicides to form fungicidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present disclosure are often applied in conjunction with one or more other fungicides to control a wider variety of undesirable diseases. When used in conjunction with other fungicide(s), the presently claimed compounds may be formulated with the other fungicide(s), tank-mixed with the other fungicide(s) or applied sequentially with the other fungicide(s). Such other fungicides may include 2-(thiocyanatomethylthio)-benzothiazole, 2-phenylphenol, 8-hydroxyquinoline sulfate, ametoctradin, amisulbrom, antimycin, Ampelomyces quisqualis, azaconazole, azoxystrobin, Bacillus subtilis, Bacillus subtilis strain QST713, benalaxyl, benomyl, benthiavalicarb-isopropyl, benzovindiflupyr, benzylaminobenzene-sulfonate (BABS) salt, bicarbonates, biphenyl, bismerthiazol, bitertanol, bixafen, blasticidin-S, borax, Bordeaux mixture, boscalid, bromuconazole, bupirimate, calcium polysulfide, captafol, captan, carbendazim, carboxin, carpropamid, carvone, chlazafenone, chloroneb, chlorothalonil, chlozolinate, Coniothyrium minitans, copper hydroxide, copper octanoate, copper oxychloride, copper sulfate, copper sulfate (tribasic), coumoxystrobin, cuprous oxide, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dazomet, debacarb, diammonium ethylenebis-(dithiocarbamate), dichlofluanid, dichlorophen, diclocymet, diclomezine, dichloran, diethofencarb, difenoconazole, difenzoquat ion, diflumetorim, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinobuton, dinocap, diphenylamine, dipymetitrone, dithianon, dodemorph, dodemorph acetate, dodine, dodine free base, edifenphos, enestrobin, enestroburin, enoxastrobin, epoxiconazole, ethaboxam, ethoxyquin, etridiazole, famoxadone, fenamidone, fenaminostrobin, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, fentin, fentin acetate, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flufenoxystrobin, flumorph, fluopicolide, fluopyram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, formaldehyde, fosetyl, fosetyl-aluminium, fuberidazole, furalaxyl, furametpyr, guazatine, guazatine acetates, GY-81, hexachlorobenzene, hexaconazole, hymexazol, imazalil, imazalil sulfate, imibenconazole, iminoctadine, iminoctadine triacetate, iminoctadine tris(albesilate), iodocarb, ipconazole, ipfenpyrazolone, iprobenfos, iprodione, iprovalicarb, isofetamid, isoprothiolane, isopyrazam, isotianil, kasugamycin, kasugamycin hydrochloride hydrate, kresoxim-methyl, laminarin, mancopper, mancozeb, mandestrobin, mandipropamid, maneb, mefenoxam, mepanipyrim, mepronil, meptyl-dinocap, mercuric chloride, mercuric oxide, mercurous chloride, metalaxyl, metalaxyl-M, metam, metam-ammonium, metam-potassium, metam-sodium, metconazole, methasulfocarb, methyl iodide, methyl isothiocyanate, metiram, metominostrobin, metrafenone, mildiomycin, myclobutanil, nabam, nitrothal-isopropyl, nuarimol, octhilinone, ofurace, oleic acid (fatty acids), orysastrobin, oxadixyl, oxathiapiprolin, oxine-copper, oxpoconazole fumarate, oxycarboxin, pefurazoate, penconazole, pencycuron, penflufen, pentachlorophenol, pentachlorophenyl laurate, penthiopyrad, phenylmercury acetate, phosphonic acid, phthalide, picarbutrazox, picoxystrobin, polyoxin B, polyoxins, polyoxorim, potassium bicarbonate, potassium hydroxyquinoline sulfate, probenazole, prochloraz, procymidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, proquinazid, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyraziflumid, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyrisoxazole, pyroquilon, quinoclamine, quinoxyfen, quintozene, Reynoutria sachalinensis extract, sedaxane, silthiofam, simeconazole, sodium 2-phenylphenoxide, sodium bicarbonate, sodium pentachlorophenoxide, spiroxamine, sulfur, SYP-Z048, tar oils, tebuconazole, tebufloquin, tecnazene, tetraconazole, thiabendazole, thifluzamide, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, tolprocarb, tolylfluanid, triadimefon, triadimenol, triazoxide, triclopyricarb, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin, valifenalate, valiphenal, vinclozolin, zineb, ziram, zoxamide, Candida oleophila, Fusarium oxysporum, Gliocladium spp., Phlebiopsis gigantea, Streptomyces griseoviridis, Trichoderma spp., (RS)—N-(3,5-dichlorophenyl)-2-(methoxymethyl)-succinimide, 1,2-dichloropropane, 1,3-dichloro-1,1,3,3-tetrafluoroacetone hydrate, 1-chloro-2,4-dinitronaphthalene, 1-chloro-2-nitropropane, 2-(2-heptadecyl-2-imidazolin-1-yl)ethanol, 2,3-dihydro-5-phenyl-1,4-dithi-ine 1,1,4,4-tetraoxide, 2-methoxyethylmercury acetate, 2-methoxyethylmercury chloride, 2-methoxyethylmercury silicate, 3-(4-chlorophenyl)-5-methylrhodanine, 4-(2-nitroprop-1-enyl)phenyl thiocyanateme, ampropylfos, anilazine, azithiram, barium polysulfide, Bayer 32394, benodanil, benquinox, bentaluron, benzamacril, benzamacril-isobutyl, benzamorf, binapacryl, bis(methylmercury) sulfate, bis(tributyltin) oxide, buthiobate, cadmium calcium copper zinc chromate sulfate, carbamorph, CECA, chlobenthiazone, chloraniformethan, chlorfenazole, chlorquinox, climbazole, copper bis(3-phenylsalicylate), copper zinc chromate, cufraneb, cupric hydrazinium sulfate, cuprobam, cyclafuramid, cypendazole, cyprofuram, decafentin, dichlone, dichlozoline, diclobutrazol, dimethirimol, dinocton, dinosulfon, dinoterbon, dipyrithione, ditalimfos, dodicin, drazoxolon, EBP, ESBP, etaconazole, etem, ethirim, fenaminosulf, fenapanil, fenitropan, fluotrimazole, furcarbanil, furconazole, furconazole-cis, furmecyclox, furophanate, glyodine, griseofulvin, halacrinate, Hercules 3944, hexylthiofos, ICIA0858, isopamphos, isovaledione, mebenil, mecarbinzid, metazoxolon, methfuroxam, methylmercury dicyandiamide, metsulfovax, milneb, mucochloric anhydride, myclozolin, N-3,5-dichlorophenyl-succinimide, N-3-nitrophenylitaconimide, natamycin, N-ethylmercurio-4-toluenesulfonanilide, nickel bis(dimethyldithiocarbamate), OCH, phenylmercury dimethyldithiocarbamate, phenylmercury nitrate, phosdiphen, prothiocarb, prothiocarb hydrochloride, pyracarbolid, pyridinitril, pyroxychlor, pyroxyfur, quinacetol, quinacetol sulfate, quinazamid, quinconazole, rabenzazole, salicylanilide, SSF-109, sultropen, tecoram, thiadifluor, thicyofen, thiochlorfenphim, thiophanate, thioquinox, tioxymid, triamiphos, triarimol, triazbutil, trichlamide, urbacid, zarilamid, and any combinations thereof.

Additionally, the compounds described herein may be combined with other pesticides, including insecticides, nematocides, miticides, arthropodicides, bactericides or combinations thereof that are compatible with the compounds of the present disclosure in the medium selected for application, and not antagonistic to the activity of the present compounds to form pesticidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present disclosure may be applied in conjunction with one or more other pesticides to control a wider variety of undesirable pests. When used in conjunction with other pesticides, the presently claimed compounds may be formulated with the other pesticide(s), tank-mixed with the other pesticide(s) or applied sequentially with the other pesticide(s). Typical insecticides include, but are not limited to: 1,2-dichloropropane, abamectin, acephate, acetamiprid, acethion, acetoprole, acrinathrin, acrylonitrile, afidopyropen, alanycarb, aldicarb, aldoxycarb, aldrin, allethrin, allosamidin, allyxycarb, alpha-cypermethrin, alpha-ecdysone, alpha-endosulfan, amidithion, aminocarb, amiton, amiton oxalate, amitraz, anabasine, athidathion, azadirachtin, azamethiphos, azinphos-ethyl, azinphos-methyl, azothoate, barium hexafluorosilicate, barthrin, bendiocarb, benfuracarb, bensultap, beta-cyfluthrin, beta-cypermethrin, bifenthrin, bioallethrin, bioethanomethrin, biopermethrin, bistrifluron, borax, boric acid, broflanilide, bromfenvinfos, bromocyclen, bromo-DDT, bromophos, bromophos-ethyl, bufencarb, buprofezin, butacarb, butathiofos, butocarboxim, butonate, butoxycarboxim, cadusafos, calcium arsenate, calcium polysulfide, camphechlor, carbanolate, carbaryl, carbofuran, carbon disulfide, carbon tetrachloride, carbophenothion, carbosulfan, cartap, cartap hydrochloride, chlorantraniliprole, chlorbicyclen, chlordane, chlordecone, chlordimeform, chlordimeform hydrochloride, chlorethoxyfos, chlorfenapyr, chlorfenvinphos, chlorfluazuron, chlormephos, chloroform, chloropicrin, chlorphoxim, chlorprazophos, chlorpyrifos, chlorpyrifos-methyl, chlorthiophos, chromafenozide, cinerin I, cinerin II, cinerins, cismethrin, clacyfos, cloethocarb, closantel, clothianidin, copper acetoarsenite, copper arsenate, copper naphthenate, copper oleate, coumaphos, coumithoate, crotamiton, crotoxyphos, crufomate, cryolite, cyanofenphos, cyanophos, cyanthoate, cyantraniliprole, cyclaniliprole, cyclethrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin, cyphenothrin, cyromazine, cythioate, DDT, decarbofuran, deltamethrin, demephion, demephion-O, demephion-S, demeton, demeton-methyl, demeton-O, demeton-O-methyl, demeton-S, demeton-S-methyl, demeton-S-methylsulphon, diafenthiuron, dialifos, diatomaceous earth, diazinon, dicapthon, dichlofenthion, dichlorvos, dicloromezotiaz, dicresyl, dicrotophos, dicyclanil, dieldrin, diflubenzuron, dilor, dimefluthrin, dimefox, dimetan, dimethoate, dimethrin, dimethylvinphos, dimetilan, dinex, dinex-diclexine, dinoprop, dinosam, dinotefuran, diofenolan, dioxabenzofos, dioxacarb, dioxathion, disulfoton, dithicrofos, d-limonene, DNOC, DNOC-ammonium, DNOC-potassium, DNOC-sodium, doramectin, ecdysterone, emamectin, emamectin benzoate, EMPC, empenthrin, endosulfan, endothion, endrin, EPN, epofenonane, eprinomectin, esdepallethrine, esfenvalerate, etaphos, ethiofencarb, ethion, ethiprole, ethoate-methyl, ethoprophos, ethyl formate, ethyl-DDD, ethylene dibromide, ethylene dichloride, ethylene oxide, etofenprox, etrimfos, EXD, famphur, fenamiphos, fenazaflor, fenchlorphos, fenethacarb, fenfluthrin, fenitrothion, fenobucarb, fenoxacrim, fenoxycarb, fenpirithrin, fenpropathrin, fensulfothion, fenthion, fenthion-ethyl, fenvalerate, fipronil, flometoquin, flonicamid, flubendiamide, flucofuron, flucycloxuron, flucythrinate, flufenerim, flufenoxuron, flufenprox, flufiprole, fluhexafon, flupyradifurone, fluvalinate, fonofos, formetanate, formetanate hydrochloride, formothion, formparanate, formparanate hydrochloride, fosmethilan, fospirate, fosthietan, furathiocarb, furethrin, gamma-cyhalothrin, gamma-HCH, halfenprox, halofenozide, HCH, HEOD, heptachlor, heptafluthrin, heptenophos, heterophos, hexaflumuron, HHDN, hydramethylnon, hydrogen cyanide, hydroprene, hyquincarb, imidacloprid, imiprothrin, indoxacarb, iodomethane, IPSP, isazofos, isobenzan, isocarbophos, isodrin, isofenphos, isofenphos-methyl, isoprocarb, isoprothiolane, isothioate, isoxathion, ivermectin, jasmolin I, jasmolin II, jodfenphos, juvenile hormone I, juvenile hormone II, juvenile hormone III, kappa-bifenthrin, kappa-tefluthrin, kelevan, kinoprene, lambda-cyhalothrin, lead arsenate, lepimectin, leptophos, lindane, lirimfos, lufenuron, lythidathion, malathion, malonoben, mazidox, mecarbam, mecarphon, menazon, mephosfolan, mercurous chloride, mesulfenfos, metaflumizone, methacrifos, methamidophos, methidathion, methiocarb, methocrotophos, methomyl, methoprene, methoxychlor, methoxyfenozide, methyl bromide, methyl isothiocyanate, methylchloroform, methylene chloride, metofluthrin, metolcarb, metoxadiazone, mevinphos, mexacarbate, milbemectin, milbemycin oxime, mipafox, mirex, molosultap, momfluorothrin, monocrotophos, monomehypo, monosultap, morphothion, moxidectin, naftalofos, naled, naphthalene, nicotine, nifluridide, nitenpyram, nithiazine, nitrilacarb, novaluron, noviflumuron, omethoate, oxamyl, oxydemeton-methyl, oxydeprofos, oxydisulfoton, para-dichlorobenzene, parathion, parathion-methyl, penfluron, pentachlorophenol, permethrin, phenkapton, phenothrin, phenthoate, phorate, phosalone, phosfolan, phosmet, phosnichlor, phosphamidon, phosphine, phoxim, phoxim-methyl, pirimetaphos, pirimicarb, pirimiphos-ethyl, pirimiphos-methyl, potassium arsenite, potassium thiocyanate, pp′-DDT, prallethrin, precocene I, precocene II, precocene I, primidophos, profenofos, profluralin, promacyl, promecarb, propaphos, propetamphos, propoxur, prothidathion, prothiofos, prothoate, protrifenbute, pyflubumide, pyraclofos, pyrafluprole, pyrazophos, pyresmethrin, pyrethrin I, pyrethrin II, pyrethrins, pyridaben, pyridalyl, pyridaphenthion, pyrifluquinazon, pyrimidifen, pyriminostrobin, pyrimitate, pyriprole, pyriproxyfen, quassia, quinalphos, quinalphos-methyl, quinothion, rafoxanide, resmethrin, rotenone, ryania, sabadilla, schradan, selamectin, silafluofen, silica gel, sodium arsenite, sodium fluoride, sodium hexafluorosilicate, sodium thiocyanate, sophamide, spinetoram, spinosad, spiromesifen, spirotetramat, sulcofuron, sulcofuron-sodium, sulfluramid, sulfotep, sulfoxaflor, sulfuryl fluoride, sulprofos, tau-fluvalinate, tazimcarb, TDE, tebufenozide, tebufenpyrad, tebupirimfos, teflubenzuron, tefluthrin, temephos, TEPP, terallethrin, terbufos, tetrachloroethane, tetrachlorvinphos, tetramethrin, tetramethylfluthrin, tetraniliprole, theta-cypermethrin, thiacloprid, thiamethoxam, thicrofos, thiocarboxime, thiocyclam, thiocyclam oxalate, thiodicarb, thiofanox, thiometon, thiosultap, thiosultap-disodium, thiosultap-monosodium, thuringiensin, tioxazafen, tolfenpyrad, tralomethrin, transfluthrin, transpermethrin, triarathene, triazamate, triazophos, trichlorfon, trichlormetaphos-3, trichloronat, trifenofos, triflumezopyrim, triflumuron, trimethacarb, triprene, vamidothion, vaniliprole, XMC, xylylcarb, zeta-cypermethrin, zolaprofos, and any combinations thereof.

Additionally, the compounds described herein may be combined with herbicides that are compatible with the compounds of the present disclosure in the medium selected for application, and not antagonistic to the activity of the present compounds to form pesticidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present disclosure may be applied in conjunction with one or more herbicides to control a wide variety of undesirable plants. When used in conjunction with herbicides, the presently claimed compounds may be formulated with the herbicide(s), tank-mixed with the herbicide(s) or applied sequentially with the herbicide(s). Typical herbicides include, but are not limited to: 4-CPA; 4-CPB; 4-CPP; 2,4-D; 3,4-DA; 2,4-DB; 3,4-DB; 2,4-DEB; 2,4-DEP; 3,4-DP; 2,3,6-TBA; 2,4,5-T; 2,4,5-TB; acetochlor, acifluorfen, aclonifen, acrolein, alachlor, allidochlor, alloxydim, allyl alcohol, alorac, ametridione, ametryn, amibuzin, amicarbazone, amidosulfuron, aminocyclopyrachlor, aminopyralid, amiprofos-methyl, amitrole, ammonium sulfamate, anilofos, anisuron, asulam, atraton, atrazine, azafenidin, azimsulfuron, aziprotryne, barban, BCPC, beflubutamid, benazolin, bencarbazone, benfluralin, benfuresate, bensulfuron, bensulide, bentazone, benzadox, benzfendizone, benzipram, benzobicyclon, benzofenap, benzofluor, benzoylprop, benzthiazuron, bicyclopyrone, bifenox, bilanafos, bispyribac, borax, bromacil, bromobonil, bromobutide, bromofenoxim, bromoxynil, brompyrazon, butachlor, butafenacil, butamifos, butenachlor, buthidazole, buthiuron, butralin, butroxydim, buturon, butylate, cacodylic acid, cafenstrole, calcium chlorate, calcium cyanamide, cambendichlor, carbasulam, carbetamide, carboxazole, chlorprocarb, carfentrazone, CDEA, CEPC, chlomethoxyfen, chloramben, chloranocryl, chlorazifop, chlorazine, chlorbromuron, chlorbufam, chloreturon, chlorfenac, chlorfenprop, chlorflurazole, chlorflurenol, chloridazon, chlorimuron, chlornitrofen, chloropon, chlorotoluron, chloroxuron, chloroxynil, chlorpropham, chlorsulfuron, chlorthal, chlorthiamid, cinidon-ethyl, cinmethylin, cinosulfuron, cisanilide, clethodim, cliodinate, clodinafop, clofop, clomazone, clomeprop, cloprop, cloproxydim, clopyralid, cloransulam, CMA, copper sulfate, CPMF, CPPC, credazine, cresol, cumyluron, cyanatryn, cyanazine, cycloate, cyclopyrimorate, cyclosulfamuron, cycloxydim, cycluron, cyhalofop, cyperquat, cyprazine, cyprazole, cypromid, daimuron, dalapon, dazomet, delachlor, desmedipham, desmetryn, di-allate, dicamba, dichlobenil, dichloralurea, dichlormate, dichlorprop, dichlorprop-P, diclofop, diclosulam, diethamquat, diethatyl, difenopenten, difenoxuron, difenzoquat, diflufenican, diflufenzopyr, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimexano, dimidazon, dinitramine, dinofenate, dinoprop, dinosam, dinoseb, dinoterb, diphenamid, dipropetryn, diquat, disul, dithiopyr, diuron, DMPA, DNOC, DSMA, EBEP, eglinazine, endothal, epronaz, EPTC, erbon, esprocarb, ethalfluralin, ethametsulfuron, ethidimuron, ethiolate, ethofumesate, ethoxyfen, ethoxysulfuron, etinofen, etnipromid, etobenzanid, EXD, fenasulam, fenoprop, fenoxaprop, fenoxaprop-P, fenoxasulfone, fenquinotrione, fenteracol, fenthiaprop, fentrazamide, fenuron, ferrous sulfate, flamprop, flamprop-M, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazolate, flucarbazone, flucetosulfuron, fluchloralin, flufenacet, flufenican, flufenpyr, flumetsulam, flumezin, flumiclorac, flumioxazin, flumipropyn, fluometuron, fluorodifen, fluoroglycofen, fluoromidine, fluoronitrofen, fluothiuron, flupoxam, flupropacil, flupropanate, flupyrsulfuron, fluridone, flurochloridone, fluroxypyr, flurtamone, fluthiacet, fomesafen, foramsulfuron, fosamine, furyloxyfen, glufosinate, glufosinate-P, glyphosate, halauxifen, halosafen, halosulfuron, haloxydine, haloxyfop, haloxyfop-P, hexachloroacetone, hexaflurate, hexazinone, imazamethabenz, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, indanofan, indaziflam, iodobonil, iodomethane, iodosulfuron, iofensulfuron, ioxynil, ipazine, ipfencarbazone, iprymidam, isocarbamid, isocil, isomethiozin, isonoruron, isopolinate, isopropalin, isoproturon, isouron, isoxaben, isoxachlortole, isoxaflutole, isoxapyrifop, karbutilate, ketospiradox, lactofen, lenacil, linuron, MAA, MAMA, MCPA, MCPA-thioethyl, MCPB, mecoprop, mecoprop-P, medinoterb, mefenacet, mefluidide, mesoprazine, mesosulfuron, mesotrione, metam, metamifop, metamitron, metazachlor, metazosulfuron, metflurazon, methabenzthiazuron, methalpropalin, methazole, methiobencarb, methiozolin, methiuron, methometon, methoprotryne, methyl bromide, methyl isothiocyanate, methyldymron, metobenzuron, metobromuron, metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, molinate, monalide, monisouron, monochloroacetic acid, monolinuron, monuron, morfamquat, MSMA, naproanilide, napropamide, napropamide-M, naptalam, neburon, nicosulfuron, nipyraclofen, nitralin, nitrofen, nitrofluorfen, norflurazon, noruron, OCH, orbencarb, ortho-dichlorobenzene, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxapyrazon, oxasulfuron, oxaziclomefone, oxyfluorfen, parafluron, paraquat, pebulate, pelargonic acid, pendimethalin, penoxsulam, pentachlorophenol, pentanochlor, pentoxazone, perfluidone, pethoxamid, phenisopham, phenmedipham, phenmedipham-ethyl, phenobenzuron, phenylmercury acetate, picloram, picolinafen, pinoxaden, piperophos, potassium arsenite, potassium azide, potassium cyanate, pretilachlor, primisulfuron, procyazine, prodiamine, profluazol, profluralin, profoxydim, proglinazine, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propyrisulfuron, propyzamide, prosulfalin, prosulfocarb, prosulfuron, proxan, prynachlor, pydanon, pyraclonil, pyraflufen, pyrasulfotole, pyrazolynate, pyrazosulfuron, pyrazoxyfen, pyribenzoxim, pyributicarb, pyriclor, pyridafol, pyrdate, pyriftalid, pyriminobac, pyrimisulfan, pyrithiobac, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quinonamid, quizalofop, quizalofop-P, rhodethanil, rimsulfuron, saflufenacil, S-metolachlor, sebuthylazine, secbumeton, sethoxydim, siduron, simazine, simeton, simetryn, SMA, sodium arsenite, sodium azide, sodium chlorate, sulcotrione, sulfallate, sulfentrazone, sulfometuron, sulfosulfuron, sulfuric acid, sulglycapin, swep, TCA, tebutam, tebuthiuron, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbuchlor, terbumeton, terbuthylazine, terbutryn, tetrafluron, thenylchlor, thiazafluron, thiazopyr, thidiazimin, thidiazuron, thiencarbazone-methyl, thifensulfuron, thiobencarb, tiafenacil, tiocarbazil, tioclorim, tolpyralate, topramezone, tralkoxydim, triafamone, tri-allate, triasulfuron, triaziflam, tribenuron, tricamba, triclopyr, tridiphane, trietazine, trifloxysulfuron, trifludimoxazin, trifluralin, triflusulfuron, trifop, trifopsime, trihydroxytriazine, trimeturon, tripropindan, tritac, tritosulfuron, vernolate, and xylachlor.

Another embodiment of the present disclosure is a method for the control or prevention of fungal attack. This method comprises applying to the soil, plant, roots, foliage, or locus of the fungus, or to a locus in which the infestation is to be prevented (for example applying to cereal or grape plants), a fungicidally effective amount of one or more of the compounds of Formula I. The compounds are suitable for treatment of various plants at fungicidal levels, while exhibiting low phytotoxicity. The compounds may be useful both in a protectant and/or an eradicant fashion.

The compounds have been found to have significant fungicidal effect particularly for agricultural use. Many of the compounds are particularly effective for use with agricultural crops and horticultural plants.

It will be understood by those skilled in the art that the efficacy of the compound for the foregoing fungi establishes the general utility of the compounds as fungicides.

The compounds have broad ranges of activity against fungal pathogens. Exemplary pathogens may include, but are not limited to, causing agent of wheat leaf blotch (Zymoseptoria tritici), wheat brown rust (Puccinia triticina), wheat stripe rust (Puccinia striiformis), scab of apple (Venturia inaequalis), powdery mildew of grapevine (Uncimula necator), barley scald (Rhynchosporium secalis), blast of rice (Pyricularia oryzae), rust of soybean (Phakopsora pachyrhizi), glume blotch of wheat (Leptosphaeria nodorum), powdery mildew of wheat (Blumreria graminis f. sp. tritici), powdery mildew of barley (Blumeria graminis f. sp. hordei), powdery mildew of cucurbits (Erysiphe cichoracearum), anthracnose of cucurbits (Colletotrichum lagenarium), leaf spot of beet (Cercospora beticola), early blight of tomato (Alternaria solani), and spot blotch of barley (Cochliobolus sativus). The exact amount of the active material to be applied is dependent not only on the specific active material being applied, but also on the particular action desired, the fungal species to be controlled, and the stage of growth thereof, as well as the part of the plant or other product to be contacted with the compound. Thus, all the compounds, and formulations containing the same, may not be equally effective at similar concentrations or against the same fungal species.

The compounds are effective in use with plants in a disease-inhibiting and phytologically acceptable amount. The term “disease-inhibiting and phytologically acceptable amount” refers to an amount of a compound that kills or inhibits the plant disease for which control is desired, but is not significantly toxic to the plant. This amount will generally be from about 0.1 to about 1000 ppm (parts per million), with 1 to 500 ppm being preferred. The exact concentration of compound required varies with the fungal disease to be controlled, the type of formulation employed, the method of application, the particular plant species, climate conditions, and the like. A suitable application rate is typically in the range from about 0.10 to about 4 pounds/acre (about 0.01 to 0.45 grams per square meter, g/m²).

Any range or desired value given herein may be extended or altered without losing the effects sought, as is apparent to the skilled person for an understanding of the teachings herein.

The compounds of Formula I may be made using well-known chemical procedures. Intermediates not specifically mentioned in this disclosure are either commercially available, may be made by routes disclosed in the chemical literature, or may be readily synthesized from commercial starting materials utilizing standard procedures.

General Schemes

The following schemes illustrate approaches to generating picolinamide compounds of Formula I. The following descriptions and examples are provided for illustrative purposes and should not be construed as limiting in terms of substituents or substitution patterns.

Compounds of Formula 1.1, wherein R₃ and R₁₂ are as originally defined and are equivalent, can be prepared by the methods shown in Scheme 1, step a. The compound of Formula 1.0 can be treated with an organometallic nucleophile such as phenylmagnesium bromide (PhMgBr) in a polar aprotic solvent such as tetrahydrofuran (THF) at a temperature of about 0° C. to 23° C. to afford compounds of Formula 1.1, wherein R₃ and R₁₂ are as previously defined, as shown in a.

Compounds of Formula 2.2, wherein R₃ is as originally defined and may or may not be equal to R₁₂, can be prepared by the methods shown in Scheme 2, steps a-c. Compounds of Formula 2.2, wherein R₃ and R₁₂ are as previously defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the compounds of Formula 2.0, wherein R₃ and R₁₂ are as previously defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, with a mixture of a hydride reagent, such as triethylsilane (Et₃SiH), and an acid, such as 2,2,2-trifluoroacetic acid (TFA) in a halogenated solvent such as dichloromethane (DCM) at a temperature of about 0° C. to 23° C., as depicted in a. Alternatively, compounds of Formula 2.1, wherein R₃ and R₁₂ are an electron-deficient aryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the compounds of Formula 2.0, wherein R₃ and R₁₂ are an electron-deficient aryl or heteroaryl group and may or may not be equivalent, with a base, such as sodium hydride (NaH), and a catalyst, such as imidazole, in a polar aprotic solvent such as THF at a temperature of about 23° C., followed by sequential addition of carbon disulfide (CS₂) and an alkyl iodide, such as iodomethane (MeI), as depicted in b. Compounds of Formula 2.2, wherein R₃ and R₁₂ are an electron-deficient aryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the compounds of Formula 2.1, wherein R₃ and R₁₂ are as previously defined and may or may not be equivalent, with a tin reagent, such as tributyltin hydride, and a radical initiator, such as azobisisobutyronitrile (AIBN), in a nonpolar solvent such as toluene at a temperature of about 115° C., as depicted in c.

Compounds of Formula 3.1, wherein R₃ and R₁₂ are as originally defined and may or may not be equivalent, can be prepared according to the method outlined in Scheme 3, step a. Compounds of Formula 3.1, wherein R₃ and R₁₂ are as originally defined and may or may not be equivalent, can be prepared from compounds of Formula 3.0, wherein R₃ and R₁₂ are as previously defined and may or may not be equivalent, by treating with a base, such as NaH and an alkyl halide, such as MeI, in a polar aprotic solvent like N,N-dimethylformamide (DMF) at a temperature of about 0° C. to 23° C., as depicted in a.

Compounds of Formula 4.1, wherein R₃ and R₁₂ are as originally defined and may or may not be equivalent, can be prepared according to the method outlined in Scheme 4, step a. Compounds of Formula 4.1, wherein R₃ and R₁₂ are as originally defined and may or may not be equivalent, can be prepared from compounds of Formula 4.0, wherein R₃ and R₁₂ are as previously defined and may or may not be equivalent, by treating with a fluorination reagent, such as (diethylamino)sulfur trifluoride (DAST), in a halogenated solvent such as DCM at a temperature of about 0° C. to 23° C., as depicted in a.

Compounds of Formula 5.3, wherein R₃, R₄, and R₁₂ are as originally defined and R₃ may or may not be equivalent to R₁₂, can be prepared according to the methods outlined in Scheme 5, steps a-c. Compounds of Formula 5.3, wherein R₃, R₄, and R₁₂ are as originally defined and R₃ may or may not be equivalent to R₁₂, can be prepared from compounds of Formula 5.0, wherein R₃, R₄, and R₁₂ are as originally defined and R₃ may or may not be equivalent to R₁₂, by treating with a catalyst such as palladium on carbon (Pd/C) in a mixture of an unsaturated hydrocarbon solvent, such as cyclohexene, and a polar protic solvent, such as ethanol (EtOH), at an elevated temperature of about 65° C., as shown in a. Alternatively, compounds of Formula 5.3, wherein R₃ and R₁₂ are an electron-deficient aryl or heteroaryl group and may or may not be equivalent and R₄ is hydroxyl (OH) or alkoxy, can be obtained by treating compounds of Formula 5.1, wherein R₃, R₄, and R₁₂ are as previously defined and R₃ may or may not be equivalent to R₁₂, with a mixture of a hydride reagent, such as Et₃SiH, and an acid, such as TFA in a halogenated solvent such as DCM at a temperature of about 0° C. to 23° C., as indicated in b. Additionally, compounds of Formula 5.3, wherein R₃ and R₁₂ are as originally defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, and R₄ is a proton (H), can be obtained by treating the compounds of Formula 5.2, wherein R₃, R₄, and R₁₂ are as previously defined and R₃ may or may not be equivalent to R₁₂, with a mixture of a hydride reagent, such as Et₃SiH, and an acid, such as TFA in a halogenated solvent such as DCM at a temperature of about 0° C. to 23° C., as depicted in c.

Compounds of Formula 6.2, wherein R₃ and R₁₂ are an electron-deficient aryl or heteroaryl group and equivalent, can be prepared according to the methods outlined in Scheme 6, steps a-b. Compounds of Formula 6.1, wherein R₃ and R₁₂ are as described previously, can be prepared from compound of Formula 6.0, by treating with an aryl bromide, such as 4-bromobenzonitrile, in the presence of a Pd catalyst, such as XPhos Pd G3 (CAS #1445085-55-1, commercially available from Sigma-Aldrich), in a polar aprotic solvent such as THF at a temperature of about 55° C., as indicated in a. Compounds of Formula 6.2, wherein R₃ and R₁₂ are as described previously, can be prepared from compound of Formula 6.1, wherein R₃ and R₁₂ are as described previously, by treating with a hydride reagent, such as borane dimethyl sulfide complex, in the presence of a catalyst, such as (R)-(+)-2-Methyl-CBS-oxazaborolidine, in a polar protic solvent, such as methanol (MeOH), at a temperature of about 0° C., as indicated in b.

Compounds of Formula 7.2, wherein R₃ and R₁₂ are as originally defined and equivalent, can be prepared according to the methods outlined in Scheme 7, steps a-b. Compounds of Formula 7.1, wherein R₃ and R₁₂ are as described previously, can be prepared from compounds of Formula 7.0, by treating with a catalyst, such as SbCl₅, in a halogenated solvent such as DCM at a temperature of about 23° C., as indicated in a. Compounds of Formula 7.2, wherein R₃ and R₁₂ are as described previously, can be prepared from compound of Formula 7.1, wherein R₃ and R₁₂ are as described previously, by treating with a hydride reagent, such as borane dimethyl sulfide complex, in the presence of a catalyst, such as (R)-(+)-2-Methyl-CBS-oxazaborolidine, in a polar protic solvent, such as methanol (MeOH), at a temperature of about 23° C., as indicated in b.

Compounds of Formula 8.1, wherein n is either 0 or 1, and W is either CH₂ or O, can be prepared according to the method outlined in Scheme 8, step a. Compounds of Formula 8.1, wherein n is either 0 or 1, and W is either CH₂ or 0, can be prepared from compounds of Formula 8.0, wherein n is either 0 or 1, and W is either CH₂ or O, by treating with a base, such as n-butyllithium (n-BuLi), and an aldehyde, such as acetaldehyde, in a polar aprotic solvent such as THF at a temperature of about −78° C. to 23° C., as indicated in a.

Compounds of Formula 9.1, wherein R₃ and R₁₂ are as originally defined, can be prepared according to the method outlined in Scheme 9, step a. Compounds of Formula 9.1, wherein R₃ and R₁₂ are as originally defined, can be prepared from compounds of Formula 9.0, wherein R₃ is as originally defined (Formula 9.0 is either commerically available, or could be prepared from asymmetric Shi epoxidation of the corresponding E-olefin precursor, as reported in Wang, Z.-X.; Tu, Y.; Frohn, M.; Zhang, J.-R.; Shi, Y. J. Am. Chem. Soc. 1997, 119, 11224), by treating with a pre-mixed suspension of a copper(I) salt, such as copper iodide (CuI), and an organometallic nucleophile, such as 4-(trifluoromethyl)phenylmagnesium bromide in a polar aprotic solvent such as THF, at a temperature of about −78° C. to 23° C., as shown in a.

Compounds of Formula 10.2, wherein R₁, R₂, R₃, R₄ and R₁₂ are as originally defined, can be prepared according to the method outlined in Scheme 10, step a. Compounds of Formula 10.0, wherein R₁ is as originally defined, can be treated with alcohols of Formula 10.1, wherein R₂, R₃, R₄ and R₁₂ are as originally defined, and a coupling reagent such as 3-(ethyliminomethyleneamino)-N,N-dimethylpropan-1-amine hydrochloride (EDC), and a catalyst such as N,N-dimethylpyridin-4-amine (DMAP) in a halogenated solvent like DCM to afford compounds of Formula 10.2, wherein R₁, R₂, R₃, R₄ and R₁₂ are as previously defined, as shown in a.

Compounds of Formula 11.2, wherein R₁, R₂, R₃, R₄, R₆, R₁₂ and Z are as originally defined, can be prepared according to the methods outlined in Scheme 11, steps a-b. As depicted in a, compounds of Formula 11.2, wherein R₁, R₂, R₃, R₄ and R₁₂ are as originally defined, can be subjected to an acid, such as a 4 normal (N) solution of hydrogen chloride (HCl) in dioxane, in a halogenated solvent such as DCM to afford compounds of Formula 9.0, wherein R₁, R₂, R₃, R₄ and R₁₂ are as originally defined, as shown in a.

Compounds of Formula 11.0, wherein R₁, R₂, R₃, R₄ and R₁₂ are as originally defined, can be treated with compounds of Formula 11.1, wherein R₆ and Z are as originally defined, in the presence of a base, such as diisopropylethylamine (DIPEA), and a peptide coupling reagent, such as benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate (PyBOP), in an halogenated solvent like DCM, to afford compounds of Formula 11.2, wherein R₁, R₂, R₃, R₄, R₆, R₁₂ and Z are as originally defined, as shown in b.

Compounds of Formula 12.0, wherein R₁, R₂, R₃, R₄, R₆, R₇, R₁₂ and Z are as originally defined, can be prepared according to the method outlined in Scheme 12, step a. As shown in a, compounds of Formula 11.2, wherein R₁, R₂, R₃, R₄, R₆, R₁₂ and Z are as originally defined, can be treated with an appropriate alkyl halide with or without a reagent such as sodium iodide (NaI) and an alkali carbonate base, such as sodium carbonate (Na₂CO₃) or potassium carbonate (K₂CO₃), in a solvent like acetone at a temperature of about 55° C., or by treatment with an acyl halide in the presence of an amine base, such as pyridine, triethylamine (Et₃N), DMAP, or mixtures thereof, in an aprotic solvent such as DCM, at a temperature of about 23° C., to afford compounds of Formula 12.0 wherein R₁, R₂, R₃, R₄, R₆, R₇, R₁₂ and Z are as originally defined.

EXAMPLES

The chemistry in the following examples may be conducted using either enantiomer of 2-((tert-butoxycarbonyl)amino)propanoic acid (Boc-Ala-OH) or either protected (PMB or Bn) or unprotected enantiomer of ethyl lactate.

Example 1: Preparation of(S)-2-(benzyloxy)-1,1-bis(4-fluorophenyl)propan-1-ol

To a solution of(S)-ethyl 2-(benzyloxy)propanoate (2.08 grams (g), 10.0 millimoles (mmol)) in tetrahydrofuran (THF; 20 milliliters (mL)) at 0° C. was slowly added (4-fluorophenyl)magnesium bromide (31.3 mL, 25.0 mmol, 0.8 molar (M) in THF) over a 10 minute (min) period. The reaction vessel was allowed to warm slowly to room temperature over 2 hours (h), and the reaction mixture was quenched by careful addition of saturated (sat.) aqueous (aq.) ammonium chloride (NH₄Cl; 50 mL). The mixture was diluted with diethyl ether (Et₂O; 50 mL), the phases were separated, and the aq. phase was extracted with Et₂O (2×50 mL). The combined organic phases were washed with sat. aq. sodium chloride (NaCl, brine; 100 mL), dried over sodium sulfate (Na₂SO₄), filtered, and concentrated. The resulting oil was purified by flash column chromatography (silica gel (SiO₂), 045% acetone in hexanes) to afford the title compound (3.28 g, 93%) as a colorless oil; ¹H NMR (300 MHz, CDCl₃) δ 7.47-7.38 (m, 2H), 7.38-7.27 (m, 5H), 7.17-7.09 (m, 2H), 7.04-6.89 (m, 4H), 4.64 (dd, J=11.4, 0.7 Hz, 1H), 4.51-4.38 (m, 2H), 3.12 (s, 1H), 1.11 (d, J=6.1 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −116.19, −116.41; ESIMS m/z 377 ([M+Na]⁺).

Example 2A: Preparation of (S)-4,4′-(2-(benzyloxy)propane-1,1-diyl)bis(fluorobenzene)

To a solution of(S)-2-(benzyloxy)-1,1-bis(4-fluorophenyl)propan-1-ol (709 milligrams (mg), 2.00 mmol) in dichloromethane (DCM; 20 mL) at 0° C. was added triethylsilane (Et₃SiH; 3.19 mL, 20.0 mmol) followed by 2,2,2-trifluoroacetic acid (TFA; 1.53 mL, 20.0 mmol). The mixture was stirred at 0° C. for 1 h. The resulting solution was quenched by careful addition of sat. aq. sodium bicarbonate (NaHCO₃; 20 mL). The phases were separated, and the aq. phase was extracted with DCM (2×30 mL). The combined organic phases were washed with brine (50 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (627 mg, 92%) as a white solid: ¹H NMR (400 MHz, CDCl₃) δ 7.31-7.22 (m, 5H), 7.21-7.16 (m, 2H), 7.10-7.03 (m, 2H), 7.00-6.91 (m, 4H), 4.54 (dd, J=11.5, 0.7 Hz, 1H), 4.31 (dd, =11.6, 0.8 Hz, 1H), 4.14 (dq, J=8.1, 6.1 Hz, 1H), 3.93 (d, J=8.1 Hz, 1H), 1.18 (d, J=6.0 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −116.60, −117.10; ESIMS (m z) 361 ([M+Na]⁺).

Example 2B: Preparation of (S)-(2-(benzyloxy)-1-methoxypropane-1,1-diyl)dibenzene

To a suspension of sodium hydride (NaH; 52.0 mg, 1.30 mmol, 60% weight per weight (w/w) in mineral oil) in N,N-dimethylformamide (DMF; 3 mL) at 0° C. was added a solution of (S)-2-(benzyloxy)-1,1-diphenylpropan-1-ol (318 mg, 1 mmol) in DMF (1 mL). The reaction mixture was stirred at room temperature for 30 min and then cooled to 0° C. Iodomethane (MeI; 93.0 microliters (μL), 1.50 mmol) was added, and the reaction mixture was stirred at room temperature for 1 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO₃ (10 mL). The mixture was diluted with diethyl ether (Et₂O; 10 mL), the phases were separated, and the aq. phase was extracted with Et₂O (2×10 mL). The combined organic phases were washed with brine (20 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→5% acetone in hexanes) to afford the title compound (295 mg, 89%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.47-7.41 (m, 2H), 7.40-7.35 (m, 2H), 7.33-7.18 (m, 11H), 4.69 (d, J=11.9 Hz, 1H), 4.54 (d, J=12.3 Hz, 1H), 4.50 (q, J=6.1 Hz, 1H), 3.13 (s, 3H), 1.10 (d, J=6.1 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 142.96, 141.31, 138.79, 129.13, 128.54, 128.14, 127.61, 127.16, 127.08, 126.95, 126.69, 99.99, 85.35, 78.13, 70.80, 52.46, 13.65; ESIMS (m/z) 333 ([M+H]⁺).

Example 2C: Preparation of (S)-(2-(benzyloxy)-1-fluoropropane-1,1-diyl)dibenzene

To a solution of (S)-2-(benzyloxy)-1,1-diphenylpropan-1-ol (300 mg, 0.942 mmol) in DCM (5 mL) at 0° C. was added (diethylamino)sulfur trifluoride (DAST; 1.88 mL, 1.88 mmol, 1 M in DCM). The reaction was slowly warmed to room temperature over 3 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO₃ (5 mL). The phases were separated, and the aq. phase was extracted with DCM (2×10 mL). The combined organic phases were washed with brine (10 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (300 mg, 98%) as a colorless oil; ¹H NMR (400 MHz. CDCl₃) δ 7.58-7.49 (m, 2H), 7.43-7.37 (m, 2H), 7.36-7.20 (m, 9H), 7.09-6.99 (m, 2H), 4.47 (d, J=11.7 Hz, 1H), 4.37-4.25 (m, 2H), 1.26 (dd, J=6.3, 1.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 142.23 (d, J=22.7 Hz), 141.00 (d, J=23.5 Hz), 138.03, 128.21, 128.16, 127.90 (d, J=1.5 Hz), 127.80, 127.72 (d, J=1.7 Hz), 127.52, 127.42 (d, J=1.3 Hz), 126.23 (d, 0.1=9.6 Hz), 125.93 (d, J=8.7 Hz), 99.96 (d, J=180.8 Hz), 78.91 (d, J=26.9 Hz), 71.68, 14.47 (d, J=3.6 Hz); ¹⁹F NMR (376 MHz, CDCl₃) δ −159.80.

Example 2D, Step 1: Preparation of (S)—O-(2-(benzyloxy)-1,1-bis(3,4,5-trifluorophenyl)propyl)S-methyl carbonodithioate

To a solution of(S)-2-(benzyloxy)-1,1-bis(3,4,5-trifluorophenyl)propan-1-ol (496 mg, 1.16 mmol) in anhydrous THF (5.8 mL) was added NaH (93.0 mg, 2.33 mmol), followed by imidazole (3.96 mg, 0.0580 mmol), and the reaction mixture was stirred at ambient temperature for 1 h. Carbon disulfide (562 μL, 9.30 mmol) was added via syringe in one portion, followed by MeI (579 μL, 9.30 mmol), and the reaction mixture was stirred at ambient temperature for 2 h. The reaction mixture was diluted with Et₂O (5 mL) and quenched with sat. aq. NH₄Cl (10 mL). The layers were separated, and the aq. layer was extracted with Et₂O (3×10 mL). The combined organic layers were dried over magnesium sulfate (MgSO₄), filtered and concentrated to afford an orange/brown oil. The crude oil was purified by flash column chromatography (SiO₂, 0→50% ethyl acetate (EtOAc) in hexanes) to afford the title compound (627 mg, 94%) as a clear, bright yellow colored oil; ¹H NMR (400 MHz, CDCl₃) δ 7.40-7.27 (m, 3H), 7.24-7.16 (m, 2H), 7.02 (dd, J=9.1, 6.6 Hz, 2H), 6.96 (dd, J=8.8, 6.5 Hz, 2H), 5.44 (q, J=6.1 Hz, 1H), 4.66 (d, J=11.6 Hz, 1H), 4.51 (d, J=11.6 Hz, 1H), 2.49 (s, 3H), 1.16 (d, J=6.1 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −133.89 (d, J=20.7 Hz), −134.73 (d, J=20.6 Hz), −159.83 (t, J=20.6 Hz), −160.56 (t, J=20.7 Hz); (Thin film) 2922, 1721, 1622, 1595, 1526, 1436, 1344, 1241, 1217, 1197, 1119, 1088, 1040, 965, 908, 861, 822, 730, 712, 697, 672 cm⁻¹.

Example 2D, Step 2: Preparation of (S)-5,5′-(2-(benzyloxy)propane-1,1-diyl)bis(1,2,3-trifluorobenzene)

A solution of (S)—O-(2-(benzyloxy)-1,1-bis(3,4,5-trifluorophenyl)propyl)S-methyl carbonodithioate (598 mg, 1.16 mmol) in toluene (200 mL) was degassed by a freeze-pump-thaw procedure (3 cycles using liquid nitrogen (N₂)) under an atmosphere of N₂. Tributyltin hydride (3.12 mL, 11.6 mmol) was then added, the reaction flask was fitted with a reflux condenser, and the reaction mixture was heated to a light reflux (115° C.). A solution of azobisisobutyronitrile (AIBN; 0.200 g, 1.22 mmol) in degassed toluene (3 cycles via liquid N₂; 32 mL) was added via syringe down the reflux condenser over 3 h. Once slow addition of the AIBN was complete, the reaction mixture was stirred at reflux overnight. The solvent was removed in vacuo to provide a pale yellow oil. The crude oil was purified by flash column chromatography (SiO₂, 0→30% EtOAc in hexanes) to afford the title compound (358 mg, 72%) as a clear, colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.28 (d, J=6.6 Hz, 3H), 7.17-7.06 (m, 2H), 6.92 (dd, J=8.5, 6.5 Hz, 2H), 6.79 (dd, J=8.3, 6.4 Hz, 2H), 4.59 (d, J=11.7 Hz, 1H), 4.31 (d, J=11.7 Hz, 1H), 4.02 (p, J=6.2 Hz, 1H), 3.76 (d, J=6.8 Hz, 1H), 1.19 (d, J=6.1 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −133.80 (d, J=20.5 Hz), −134.34 (d, J=20.5 Hz), −162.54 (t, J=20.5 Hz), −162.84 (t, J=20.5 Hz); (Thin film) 2871, 1621, 1526, 1445, 1345, 1262, 1235, 1116, 1096, 1043, 859, 802, 728, 698, 679 cm⁻¹.

Example 3A: Preparation of (S)-1,1-bis(4-fluorophenyl)propan-2-ol

To a solution of (S)-4,4′-(2-(benzyloxy)propane-1,1-diyl)bis(fluorobenzene) (575 mg, 1.70 mmol) in ethanol (EtOH; 11 mL) and cyclohexene (5.5 mL) at room temperature was added palladium on carbon (Pd/C; 362 mg, 0.0850 mmol, 2.5% w/w of Pd). The reaction mixture was stirred at 65° C. for 2 h, cooled to room temperature, filtered through a plug of Celite®, and concentrated to afford the title compound (415 mg, 98%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.36-7.29 (m, 2H), 7.25-7.18 (m, 2H), 7.09-6.93 (m, 4H), 4.47 (dqd, J=8.2, 6.1, 3.3 Hz, 1H), 3.80 (d, J=8.3 Hz, 1H), 1.55 (d, J=3.3 Hz, 1H), 1.19 (d, J=6.1 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 162.90 (d, J=23.3 Hz), 160.46 (d, J=23.1 Hz), 138.15 (d, J=3.1 Hz), 136.94 (d, J=3.6 Hz), 130.14 (d, J=7.8 Hz), 129.55 (d, J=7.8 Hz), 115.70 (d, J=18.8 Hz), 115.49 (d, J=18.8 Hz), 70.07, 58.61, 21.63; ¹⁹F NMR (376 MHz, CDCl₃) δ −115.84, −116.19.

Example 3B: Preparation of(S)-1,1-bis(2-fluorophenyl)propane-1,2-diol

To a solution of (S)-1,1-bis(2-fluorophenyl)-2-((4-methoxybenzyl)oxy)propan-1-ol (790 mg, 2.06 mmol) in DCM (20 mL) at 0° C. was added Et₃SiH (3.28 mL, 20.6 mmol) followed by TFA (1.57 mL, 20.6 mmol). The mixture was stirred at 0° C. for 1 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO₃ (20 mL). The phases were separated, and the aq. phase was extracted with DCM (2×30 mL). The combined organic phases were washed with brine (50 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (388 mg, 71%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.90-7.77 (m, 1H), 7.70 (tt, J=8.2, 1.5 Hz, 1H), 7.31-7.10 (m, 4H), 6.97 (ddd, J=12.7, 8.1, 1.3 Hz, 1H), 6.88 (ddd, J=11.8, 8.0, 1.4 Hz, 1H), 5.11 (qd, J=6.3, 2.3 Hz, 1H), 3.49 (s, 1H), 2.27 (s, 1H), 1.09 (d, J=6.3 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −112.90 (d, J=8.3 Hz), −113.92 (d, J=8.4 Hz); ESIMS (m/z) 551 ([2M+Na]⁺).

Example 3C: Preparation of(S)-1,1-bis(4-bromophenyl)propan-2-ol

To a solution of(S)-1,1-bis(4-bromophenyl)-2-((4-methoxybenzyl)oxy)propan-1-ol (1.80 g, 3.56 mmol) in DCM (18 mL) at 0° C. was added Et₃SiH (5.68 mL, 35.6 mmol) followed by TFA (2.72 mL, 35.6 mmol). The mixture was warmed slowly to room temperature over 3 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO₃ (20 mL). The phases were separated, and the aq. phase was extracted with DCM (2×30 mL). The combined organic phases were washed with brine (50 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (742 mg, 560/%) as a colorless oil; ¹H NMR (300 MHz, CDCl₃) 7.51-7.36 (m, 4H), 7.25-7.17 (m, 2H), 7.18-7.06 (m, 2H), 4.48 (dq, J=8.2, 6.1 Hz, 1H), 3.76 (d, J=8.2 Hz, 1H), 2.80 (s, 1H), 1.19 (d, J=6.2 Hz, 3H); ¹³C NMR (75 MHz, CDCl₃) δ 140.94, 139.85, 131.98, 131.85, 130.39, 129.84, 121.06, 120.72, 69.82, 58.91, 21.65; (Thin film) 3390, 3024, 2969, 2900, 1486, 1072 cm⁻¹.

Example 3D, Step 1: Preparation of (S) 1,1-bis(4-((trimethylsilyl)ethynyl)-phenyl)propan-2-ol

To a solution of(S)-1,1-bis(4-bromophenyl)propan-2-ol (1.01 g, 2.72 mmol) in THF (9 mL) was added bis(triphenylphosphine)palladium dichloride (0.095 g, 0.136 mmol) and copper(I) iodide (CuI; 0.026 g, 0.136 mmol). The mixture was sparged with N₂ for 20 min, and triethylamine (Et₃N; 4.53 mL) was added dropwise. To the resulting mixture was added ethynyltrimethylsilane (1.15 mL, 8.15 mmol) dropwise, and the mixture was heated to reflux and stirred overnight. The mixture was cooled to room temperature, and the reaction was quenched with sat. aq. NaHCO₃. The products were extracted with EtOAc (2×), and the combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated. The crude residue was then purified by flash column chromatography (SiO₂, 0→20% acetone in hexanes) to provide the title compound (495 mg, 45%) as a brown foam; ¹H NMR (400 MHz, CDCl₃) δ 7.48-7.42 (m, 2H), 7.42-7.37 (m, 2H), 7.33-7.27 (m, 2H), 7.24-7.17 (m, 2H), 4.51 (dqd, J=12.2, 6.1, 3.5 Hz, 1H), 3.81 (d, J=8.3 Hz, 1H), 1.60 (d, J=3.8 Hz, 1H), 1.18 (d, J=6.1 Hz, 3H), 0.26 (s, 9H), 0.26 (s, 9H); ¹³C NMR (101 MHz, CDCl₃) δ 142.55, 141.48, 132.42, 132.29, 128.69, 128.15, 121.90, 121.57, 104.76, 104.71, 94.49, 94.33, 69.76, 59.96, 21.55, 0.00; (Thin film) 3397, 2960, 2156, 1501, 1248, 861, 840 cm⁻¹, HRMS-ESI (m/z) [M+H]⁺ calcd for C₂₅H₃₃OSi₂, 405.2064; found, 405.2070.

Example 3D, Step 2: Preparation of(S)-1,1-bis(4-ethynylphenyl)propan-2-ol

To a solution of(S)-1,1-bis(4-((trimethylsilyl)ethynyl)phenyl)propan-2-ol (0.470 g, 1.16 mmol) in methanol (MeOH; 5.8 mL) was added potassium carbonate (K₂CO₃; 0.482 g, 3.48 mmol). The mixture was stirred for 1 h at room temperature and then filtered through Celite®. The filter cake was washed with MeOH, and the filtrate was concentrated. The crude material was purified by flash column chromatography (SiO₂, 0→20% acetone in hexanes) to provide the title compound (288 mg, 95%) as a yellow oil; ¹H NMR (300 MHz, CDCl₃) δ 7.48-7.43 (m, 2H), 7.43-7.39 (m, 2H), 7.35-7.29 (m, 2H), 7.24-7.19 (m, 2H), 4.51 (dqd, J=8.3, 6.1, 3.7 Hz, 1H), 3.82 (d, J=8.3 Hz, 1H), 3.05 (s, 1H), 3.04 (s, 1H), 1.63-1.55 (m, 1H), 1.18 (d, J=6.1 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 142.84, 141.82, 132.60, 132.48, 128.74, 128.22, 120.87, 120.57, 83.31, 83.29, 77.39, 77.29, 69.73, 59.96, 21.66; (Thin film) 3436, 3280, 2968, 2106, 1499, 1075, 825 cm⁻¹; HRMS-ESI (m/z) [M+H]⁺ calcd for C₁₉H₁₇O, 261.1274; found, 261.1272.

Example 3D, Step 3: Preparation of (S)-1,1-bis(4-ethylphenyl)propan-2-ol

To a solution of(S)-1,1-bis(4-ethynylphenyl)propan-2-ol (0.144 g, 0.553 mmol) in EtOAc (2.8 mL) was added palladium (5% weight (wt) on carbon, dry basis; 0.235 g, 0.055 mmol). The mixture was stirred under a balloon of hydrogen overnight. The mixture was filtered through Celite®, and the filter cake was washed with EtOAc. The combined filtrate was then concentrated, and the crude residue was purified by flash column chromatography (SiO₂, 0425% acetone in hexanes) to provide the title compound (97.0 mg, 65%) as a clear oil; ¹H NMR (400 MHz, CDCl₃) δ 7.33-7.25 (m, 2H), 7.22-7.15 (m, 2H), 7.18-7.11 (m, 2H), 7.10 (d, J=8.1 Hz, 2H), 4.51 (dqd, J=8.7, 6.1, 2.5 Hz, 1H), 3.74 (d, J=8.9 Hz, 1H), 2.65-2.53 (m, 4H), 1.68 (d, J=2.8 Hz, 1H), 1.23-1.14 (m, 9H); ¹³C NMR (101 MHz, CDCl₃) δ 142.74, 142.33, 139.94, 138.91, 128.48, 128.40, 128.07, 128.02, 70.19, 60.02, 28.41, 28.39, 21.37, 15.47, 15.46; (Thin film) 3421, 2963, 1510, 1110, 821 cm⁻¹; HRMS-ESI (m/z) ([M+Na]⁺) calcd for C₁₉H₂₄NaO, 291.1719; found, 291.1725.

Example 3E: Preparation of 1-(9H-xanthen-9-yl)ethanol

To a solution of 9H-xanthene (364 mg, 2.00 mmol) in THF (10 mL) at −78° C. was added n-butyllithium (2.5 M in hexanes; 0.880 mL, 2.20 mmol). The mixture was stirred at −78° C. for 30 min. Acetaldehyde (0.226 mL, 4.00 mmol) was added, and the reaction mixture was warmed slowly to room temperature overnight. The resulting solution was quenched by careful addition of sat. aq. NH₄Cl (10 mL). The phases were separated, and the aq. phase was extracted with Et₂O (2×15 mL). The combined organic phases were washed with brine (20 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (216 mg, 48%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.33-7.22 (m, 4H), 7.17-7.04 (m, 4H), 3.99 (d, J=5.1 Hz, 1H), 3.96-3.82 (m, 1H), 1.54 (d, J=6.0 Hz, 1H), 1.00 (d, J=6.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 152.94, 152.65, 129.54, 129.30, 128.19, 128.17, 123.18, 123.14, 122.48, 121.73, 116.59, 116.41, 73.07, 47.06, 18.81; ESIMS (m z) 475 ([2M+Na]).

Example 3F: Preparation of (1S,2S)-1-phenyl-1-(4-(trifluoromethyl)phenyl)propan-2-ol

To a mixture of magnesium turnings (102 mg, 4.20 mmol) in Et₂O (4 mL) was added 1-bromo-4-(trifluoromethyl)benzene (0.588 mL, 4.20 mmol) at room temperature, followed by MeI (5 μL). Upon warming to a gentle boil using a heat gun, the mixture turned a yellow/brown color. The reaction was then stirred in a water bath at room temperature for 30 min until almost all the magnesium was consumed. This was added to a suspension of copper(I) iodide (CuI; 400 mg, 2.10 mmol) in Et₂O (4 mL) at −78° C. The reaction was stirred at −20° C. for 30 min, then cooled to −78° C., and (2S,3S)-2-methyl-3-phenyloxirane (0.201 mL, 1.50 mmol) was added. The resulting mixture was warmed slowly to room temperature overnight. The resulting solution was quenched by careful addition of sat. aq. NH₄Cl (10 mL). The phases were separated, and the aq. phase was extracted with Et₂O (2×15 mL). The combined organic phases were washed with brine (20 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→10% acetone in hexanes) to afford the title compound (390 mg, 94%) as a light yellow oil; ¹H NMR (400 MHz, CDCl₃) δ 7.60-7.50 (m, 2H), 7.48-7.38 (m, 2H), 7.38-7.33 (m, 4H), 7.30-7.23 (m, 1H), 4.58 (dqd, J=8.4, 6.1, 3.5 Hz, 1H), 3.88 (d, J=8.5 Hz, 1H), 1.65 (d, J=3.6 Hz, 1H), 1.20 (d, J=6.1 Hz, 3H); ¹⁹F NMR (376 MHz, CDCl₃) δ −62.49; ESIMS (m/z) 263 ([M−OH]⁺).

Example 3G, Step 1: Preparation of 4,4′-(2-oxopropane-1,1-diyl)dibenzonitrile

To a suspension of 4-bromobenzonitrile (546 mg, 3.00 mmol) and cesium carbonate (977 mg, 3.00 mmol) in THF (10 mL) under an N₂ atmosphere was added acetone (1.10 mL, 15.00 mmol), followed by X-Phos Pd G3 (50.8 mg, 0.060 mmol). Then, the vial was sealed and heated to 55° C. for 4 days. The reaction was diluted with EtOAc (30 mL) and washed with sat. NH₄Cl (3×10 mL), water (15 mL), and brine (15 mL). Then the organic phase was dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→40% EtOAc in hexanes) to afford the title compound (174 mg, 22%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.66 (d, 0.1=8.4 Hz, 4H), 7.34 (d, J=8.3 Hz, 4H), 5.21 (s, 1H), 2.29 (s, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 203.68, 142.15, 132.75, 129.64, 118.21, 112.00, 64.25, 30.43; ESIMS m/z 261 ([M+H]⁺).

Example 3G, Step 2: Preparation of (S)-4,4′-(2-hydroxypropane-1,1-diyl)dibenzonitrile

To a solution of 4,4′-(2-oxopropane-1,1-diyl)dibenzonitrile (174 mg, 0.668 mmol) in toluene (4.5 mL) was added (R)-1-methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole (1 M solution in toluene, 66.8 μL, 0.067 mmol). Then, the reaction was cooled to 0° C. and a solution of BH₃-DMS (69.8 μl, 0.735 mmol) in 0.5 mL toluene was added over 2 min. The flask was left to stir at 0° C. After 2 h, the reaction was quenched with methanol (0.5 mL), diluted with EtOAc and added water. Phases were separated and the aqueous phase was extracted with EtOAc×2. The combined organic phases were washed with brine (20 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→50% EtOAc in hexanes) to afford the title compound (99.7 mg, 57%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ d 7.60 (dd, J=8.4, 6.8 Hz, 4H), 7.51-7.46 (m, 2H), 7.43-7.37 (m, 2H), 4.63-4.47 (m, 1H), 3.97 (d, J=7.5 Hz, 1H), 1.97 (d, J=3.8 Hz, 1H), 1.21 (d, J=6.2 Hz, 3H). ¹³C NMR (101 MHz, CDCl₃) δ 146.91, 145.86, 132.60, 132.45, 129.90, 129.19, 118.58, 118.51, 110.96, 110.92, 69.19, 59.56, 22.27; ESIMS m/z 263 ([M+H]⁺).

Example 3H, Step 1: Preparation of 3,3-diphenylbutan-2-one

To a magnetically stirred mixture of 2,3-diphenylbutane-2,3-diol (500 mg, 2.06 mmol) in DCM (10 mL) was added antimony pentachloride (26.5 μL, 0.206 mmol) under air atmosphere. The reaction mixture was stirred at 25° C. for 1 h and then was quenched by slow addition of sat. aq. NaHCO₃. The resulting mixture was diluted with water and additional DCM, and the organic layer was separated by passing through a phase separator. The resulting oil was purified by flash column chromatography (SiO₂, 0→5% acetone in hexanes) to afford the title compound (330 mg, 71%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.36-7.31 (m, 4H), 7.30-7.25 (m, 2H), 7.23-7.15 (m, 4H), 2.11 (s, 3H), 1.87 (s, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 209.16, 143.59, 128.36, 126.91, 62.32, 27.62, 26.42; ESIMS m/z 225 ([M+H]⁺).

Example 3H, Step 2: Preparation of (S)-3,3-diphenylbutan-2-ol

To a solution of 3,3-diphenylbutan-2-one (150 mg, 0.669 mmol) in toluene 4.5 mL) was added (R)-1-methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole (1 M solution in toluene, 134 μL, 0.134 mmol). Then, a solution of BH₃-DMS (70.2 μL, 0.702 mmol) in 0.5 mL of toluene was added to the reaction mixture over 2 min. The flask was left to stir at room temperature. After 1 h, the reaction was quenched with methanol (0.5 mL). DCM and water were added, and the phases were separated. The aqueous phase was extracted with DCM (2×). The combined organic phases were washed with brine (20 mL), dried over Na₂SO₄, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO₂, 0→20% acetone in hexanes) to afford the title compound (150 mg, 99%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ d 7.39-7.17 (m, 10H), 4.70-4.61 (m, 1H), 1.67 (s, 3H), 1.51 (d, J=4.9 Hz, 1H), 1.11 (d, J=6.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 147.30, 145.86, 128.40, 128.15, 128.05, 127.79, 126.20, 126.01, 72.28, 51.77, 23.26, 18.39; ESIMS m/z 227 ([M+H]⁺).

Example 31, Step 1: Preparation of (S)-1,1-bis(2,3-dimethoxyphenyl)propane-1,2-diol

To a solution of isopropylmagnesium lithium chloride (1.3 M in THF, 6.1 mL, 8.00 mmol) was added THF (2 mL) and 1-bromo-2,3-dimethoxybenzene (1.74 g, 8.00 mmol). The resulting brown solution was heated to a gentle reflux (75° C. external temp) for 2.5 h, then cooled to 0° C. in an ice water bath. (S)-methyl 2-hydroxypropanoate (0.191 ml, 2 mmol) was then added dropwise via syringe. The reaction was stirred at 0° C. for 1 h, then removed from the cold bath and stirred overnight at rt. The reaction was cooled to 0° C. in an ice water bath, diluted with water (20 mL), brine (20 mL), and Et₂O (40 mL), and was quenched with 1 N HCl (8 mL). The phases were separated, and the aqueous phase was extracted with Et₂O (20 mL). The organic phases were combined, dried over MgSO₄, filtered, and concentrated to provide an oil. Purification by automated silica gel column chromatography (5-50% EtOAc in hexanes) provided the title compound (568 mg, 82%) as a yellow, crystalline solid; ¹H NMR (300 MHz, CDCl₃) δ 7.43 (td, J=8.0, 1.5 Hz, 2H), 7.11 (td, J=8.1, 4.9 Hz, 2H), 6.83 (dd, J=8.1, 1.4 Hz, 2H), 5.06-4.82 (m, 1H), 4.74 (d, J=1.2 Hz, 1H), 3.81 (s, 3H), 3.80 (s, 3H), 3.20 (s, 3H), 3.04 (s, 3H), 2.86 (d, J=9.5 Hz, 1H), 0.97 (d, J=6.4 Hz, 3H); ¹³C NMR (126 MHz, CDCl₃) δ 152.89, 152.82, 146.94, 145.53, 139.56, 138.92, 123.32, 123.26, 122.01, 119.01, 111.30, 79.20, 77.22, 60.07, 59.26, 55.77, 55.64, 18.34; HRMS-ESI (m/z) ([M+Na]⁺) calcd for C₁₉H₂₄O₆Na, 371.1465; found, 371.1456.

Example 31, Step 2: Preparation of 1,1-bis(2,3-dimethoxyphenyl)propan-2-one

To a solution of(S)-1,1-bis(2,3-dimethoxyphenyl)propane-1,2-diol (560 mg, 1.61 mmol) in anhydrous CH₂Cl₂ (8 mL) at 0° C. was added triethylsilane (770 μl, 4.82 mmol) and trifluoroacetic acid (TFA, 124 μL, 1.61 mmol). The resulting solution was stirred at 0° C. for 2 h, then removed from the cold bath and stirred for 2 h. TFA (248 μL, 3.2 mmol) was added, and the reaction was then stirred overnight at rt. The reaction was diluted with water (25 mL) and extracted with CH₂Cl₂ (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to provide an oil. Purification by automated silica gel column chromatography (5-25% acetone in hexanes) provided the title compound (396 mg, 75%) as a white solid; ¹H NMR (300 MHz, CDCl₃) δ 6.99 (t, J=8.0 Hz, 2H), 6.87 (dd, J=8.2, 1.5 Hz, 2H), 6.67-6.54 (m, 2H), 5.86 (s, 1H), 3.87 (s, 6H), 3.75 (s, 6H), 2.25 (s, 3H); ¹³C NMR (126 MHz, CDCl₃) δ 207.18, 152.69, 147.02, 132.23, 123.74, 121.61, 111.64, 60.36, 55.74, 51.96, 29.80; HRMS-ESI (m/z) ([M+Na]⁺) calcd for C₁₉H₂₂O₅Na, 353.1359; found, 353.1353.

Example 31, Step 3: Preparation of 1,1-bis(2,3-dimethoxyphenyl)propan-2-ol

To a solution of 1,1-bis(2,3-dimethoxyphenyl)propan-2-one (356 mg, 1.08 mmol) in methanol (3.5 mL) was added sodium borohydride (61 mg, 1.6 mmol). The resulting solution was stirred at rt for 20 h, then was quenched with sat'd NH₄Cl (1 mL), diluted with water (20 mL) and extracted with CH₂Cl₂ (3×20 mL). The organic extracts were combined, dried over Na₂SO₄, filtered, and concentrated to provide the title compound (360 mg, 100%) as an oil; ¹H NMR (300 MHz, CDCl₃) δ 7.16-6.88 (m, 4H), 6.79 (ddd, J=9.6, 7.8, 1.9 Hz, 2H), 4.81 (d, J=8.3 Hz, 1H), 4.53-4.32 (m, 1H), 3.84 (s, 3H), 3.84 (s, 3H), 3.77 (s, 3H), 3.76 (s, 3H), 2.04 (d, J=4.2 Hz, 1H), 1.22 (d, J=6.2 Hz, 3H); ¹³C NMR (126 MHz, CDCl₃) δ 152.98, 152.83, 147.71, 147.04, 136.17, 135.33, 123.94, 123.62, 120.96, 120.84, 110.76, 110.48, 70.32, 60.26, 60.20, 55.66, 55.63, 45.11, 21.80; IR (neat film) 3451, 2935, 2833, 1582, 1473, 1428, 1266, 1215, 1167, 1125, 1088, 1068, 1004, 964, 908, 835, 809, 787, 748, 728.

Example 4A: Preparation of (S)—(S)-1,1-diphenylpropan-2-yl 2-((tert-butoxycarbonyl)amino)-propanoate

To a solution of (S)-1,1-diphenylpropan-2-ol (317 mg, 1.493 mmol) in DCM (15 mL) at 0° C. were added (S)-2-((tert-butoxycarbonyl)amino)propanoic acid (Boc-Ala-OH; 311 mg, 1.64 mmol) and N,N-dimethylpyridin-4-amine (DMAP; 18.2 mg, 0.149 mmol) followed by N¹-((ethylimino)methylene)-N³,N³-dimethylpropane-1,3-diamine hydrochloride (EDC; 573 mg, 2.99 mmol), and the reaction mixture was stirred at room temperature overnight and concentrated to give a yellow oil. The crude material was purified by flash column chromatography (SiO₂, 1→10% acetone in hexanes) to afford the title compound (433 mg, 75%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 7.42-7.07 (m, 10H), 5.80 (dq, J=10.1, 6.1 Hz, 1H), 4.97 (d, J=8.0 Hz, 1H), 4.19-4.06 (m, 1H), 4.03 (d, J=10.1 Hz, 1H), 1.41 (s, 9H), 1.23 (d, J=6.1 Hz, 3H), 0.76 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) 172.83, 154.96, 141.52, 141.26, 128.79, 128.50, 128.10, 128.08, 126.91, 126.67, 79.62, 73.10, 57.98, 49.21, 28.33, 19.31, 17.98; ESIMS m/z 384 ([M+H]⁺).

Example 5, Step 1: Preparation of(S)-1-(((S)-1,1-diphenylpropan-2-yl)oxy)-1-oxopropan-2-aminium chloride

To a solution of (S)—(S)-1,1-diphenylpropan-2-yl 2-((tert-butoxycarbonyl)amino)propanoate (Cmpd 2; 433 mg, 1.13 mmol) in DCM (6 mL) was added a 4 N solution of HCl in dioxane (2.8 mL, 11.3 mmol), and the mixture was stirred for 3 h at room temperature. The solvent was evaporated under a stream of N₂ to provide the title compound (360 mg, 100%) as a white solid: ESIMS (nm/z) 284 ([M+H]⁺).

Example 5, Step 2: Preparation of(S)—(S)-1,1-diphenylpropan-2-yl 2-(3-hydroxy-4-methoxypicolinamido)propanoate

To a solution of (S)-1-(((S)-1,1-diphenylpropan-2-yl)oxy)-1-oxopropan-2-aminium chloride (Cmpd 46; 361 mg, 1.13 mmol) and 3-hydroxy-4-methoxypicolinic acid (210 mg, 1.24 mmol) in DCM (I 1 mL) were added benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate (PyBOP; 646 mg, 1.24 mmol) and N-ethyl-N-isopropylpropan-2-amine (DIPEA; 0.651 mL, 3.72 mmol), and the reaction mixture was stirred for 2 h at room temperature. The solvent was evaporated and the crude oil was purified by flash column chromatography (SiO₂, 1→50% acetone in hexanes) to afford the title compound (340 mg, 70%) as a white foam: ¹H NMR (400 MHz, CDCl₃) δ 12.10 (s, 1H), 8.34 (d, J=8.0 Hz, 1H), 7.98 (d, J=5.2 Hz, 1H), 7.38-7.06 (m, 10H), 6.86 (d, J=5.3, 1H), 5.83 (dq, J=10.1, 6.1 Hz, 1H), 4.52 (dq, J=8.1, 7.2 Hz, 1H), 4.06 (d, J=10.2 Hz, 1H), 3.93 (s, 3H), 1.26 (d, J=6.1 Hz, 3H), 0.97 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 171.67, 168.53, 155.34, 148.72, 141.38, 141.13, 140.40, 130.48, 128.80, 128.50, 128.10, 128.03, 126.95, 126.70, 109.39, 73.57, 57.93, 56.07, 47.85, 19.24, 17.61; HRMS-ESI (m/z) ([M+H]⁺) calcd for C₂₅H₂₇N₂O₅, 435.1920; found, 435.1925.

Example 6A: Preparation of (S)—(S)(S)-1,1-diphenylpropan-2-yl 2-(3-acetoxy-4-methoxypicolinamido)propanoate

To a solution of(S)—(S)-1,1-diphenylpropan-2-yl 2-(3-hydroxy-4-methoxypicolinamido)-propanoate (Cmpd 90; 70.0 mg, 0.161 mmol), Et₃N (44.9 μL, 0.332 mmol), and DMAP (3.94 mg, 0.032 mmol) in DCM (3.2 mL) was added acetyl chloride (17.2 μL, 0.242 mmol) at room temperature, and the reaction mixture was stirred for 2 h. The solvent was evaporated, and the resulting crude oil was purified by flash column chromatography (SiO₂, 1→40% acetone in hexanes) to afford the title compound (75.0 mg, 97%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 8.41 (d, J=7.8 Hz, 1H), 8.30 (d, J=5.4 Hz, 1H), 7.38-7.10 (m, 10H), 6.97 (d, J=5.4 Hz, 1H), 5.82 (dq, J=10.0, 6.2 Hz, 1H), 4.52 (dt, J=8.2, 7.1 Hz, 1H), 4.05 (d, J=10.1 Hz, 1H), 3.87 (s, 3H), 2.37 (s, 3H), 1.24 (d, J=6.1 Hz, 3H), 0.89 (d, J=7.1 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) 172.23, 168.89, 162.28, 159.42, 146.66, 141.55, 141.44, 141.25, 137.45, 128.77, 128.50, 128.13, 128.11, 126.89, 126.67, 109.73, 73.32, 57.90, 56.27, 47.85, 20.75, 19.25, 17.92; HRMS-ESI (m/z) ([M+H]⁺) calcd for C₂₇H₂₉N₂O₆, 477.2025; found, 477.2019.

Example 6B: Preparation of (S)—(S)-1,1-diphenylpropan-2-yl 2-(3-(acetoxymethoxy)-4-methoxypicolinamido)propanoate

To a suspension of(S)—(S)-1,1-diphenylpropan-2-yl 2-(3-hydroxy-4-methoxypicolinamido)-propanoate (Cmpd 90; 100 mg, 0.230 mmol) and K₂CO₃ (63.6 mg, 0.460 mmol) in acetone (4.6 mL) was added bromomethyl acetate (33.9 μL, 0.345 mmol) at room temperature, and the mixture was heated to 55° C. for 3 h and then cooled to room temperature. The solvent was evaporated and the resulting crude material was purified by flash column chromatography (SiO₂, 1→40% acetone in hexanes) to afford the title compound (94.0 mg, 80% yield) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 8.25 (d, J=5.4 Hz, 1H), 8.22 (d, J=7.9 Hz, 1H), 7.34-7.09 (m, 10H), 6.92 (d, J=5.4 Hz, 1H), 5.83 (dq, J=10.1, 6.2 Hz, 1H), 5.72 (d, J=0.7 Hz, 2H), 4.60-4.49 (m, 1H), 4.06 (d, J=10.1 Hz, 1H), 3.88 (s, 3H), 2.05 (s, 3H), 1.25 (d, J=6.1 Hz, 3H), 0.91 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 172.33, 170.25, 162.88, 160.24, 145.70, 143.91, 142.54, 141.48, 141.25, 128.76, 128.49, 128.12, 128.09, 126.89, 126.65, 109.56, 89.50, 73.27, 57.92, 56.17, 48.07, 20.86, 19.25, 17.73; HRMS-ESI (m/z) [M+H]⁺ calcd for C₂₈H₃₁N₂O₇, 507.2131; found, 507.2125.

Example 6C: Preparation of (S)—(S)-1,1-diphenylpropan-2-yl 2-(3-((isobutyryloxy)methoxy)-4-methoxypicolinamido)propanoate

To a solution of (S)—(S)-1, l-diphenylpropan-2-yl 2-(3-hydroxy-4-methoxypicolinamido)-propanoate (Cmpd 90; 100 mg, 0.230 mmol) in acetone (4.6 mL) were added sodium carbonate (Na₂CO₃; 73.2 mg, 0.690 mmol), sodium iodide (NaI; 6.90 mg, 0.046 mmol) and chloromethyl 2-ethoxyacetate (62.9 mg, 0.460 mmol). The mixture was heated to 55° C. overnight and then cooled to room temperature, and the solvent was evaporated. The resulting residue was purified by flash column chromatography (SiO₂, 2→30% acetone in hexanes) to afford the title compound (79.0 mg, 64%) as a colorless oil; ¹H NMR (400 MHz, CDCl₃) δ 8.28 (d, J=7.9 Hz, 1H), 8.25 (d, J=5.3 Hz, 1H), 7.36-7.08 (m, 10H), 6.92 (d, J=5.4 Hz, 1H), 5.83 (dq, J=10.1, 6.2 Hz, 1H), 5.79-5.69 (m, 2H), 4.62-4.44 (m, 1H), 4.06 (d, J=10.1 Hz, 1H), 3.86 (s, 3H), 2.53 (hept, J=7.0 Hz, 1H), 1.25 (d, J=6.2 Hz, 3H), 1.13 (d, J=7.0 Hz, 6H), 0.91 (d, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) 176.22, 172.34, 162.85, 160.23, 145.55, 144.16, 142.18, 141.48, 141.26, 128.76, 128.49, 128.12, 128.09, 126.89, 126.65, 109.48, 89.90, 73.26, 57.93, 56.12, 48.07, 33.85, 19.26, 18.68, 17.74; HRMS-ESI (m/z) ([M+H]⁺) calcd for C₃₀H₃₅N₂O₇, 535.2444; found, 535.2431.

Example A: Evaluation of Fungicidal Activity: Leaf Blotch of Wheat (Zyrnoseptoria tritici; Bayer Code SEPTTR)

Technical grades of materials were dissolved in acetone, which were then mixed with nine volumes of water (H₂O) containing 110 ppm Triton X-100. The fungicide solutions were applied onto wheat seedlings using an automated booth sprayer to run-off. All sprayed plants were allowed to air dry prior to further handling. All fungicides were evaluated using the aforementioned method for their activity vs. all target diseases, unless stated otherwise. Wheat leaf blotch and brown rust activity were also evaluated using track spray applications, in which case the fungicides were formulated as EC formulations, containing 0.1% Trycol 5941 in the spray solutions.

Wheat plants (variety Yuma) were grown from seed in a greenhouse in 50% mineral soil/50% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Zymoseptoria tritici either prior to or after fungicide treatments. After inoculation the plants were kept in 100% relative humidity (one day in a dark dew chamber followed by two to three days in a lighted dew chamber at 20° C.) to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse set at 20° C. for disease to develop. When disease symptoms were fully expressed on the 1^(st) leaves of untreated plants, infection levels were assessed on a scale of 0 to 100 percent disease severity. Percent disease control was calculated using the ratio of disease severity on treated plants relative to untreated plants.

Example B: Evaluation of Fungicidal Activity: Wheat Brown Rust (Puccinia triticina; Synonym: Puccinia recondita f. sp. tritici; Bayer Code PUCCRT)

Wheat plants (variety Yuma) were grown from seed in a greenhouse in 50% mineral soil/50% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Puccinia triticina either prior to or after fungicide treatments. After inoculation the plants were kept in a dark dew room at 22° C. with 100% relative humidity overnight to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse set at 24° C. for disease to develop. Fungicide formulation, application and disease assessment followed the procedures as described in the Example A.

Example C: Evaluation of Fungicidal Activity: Wheat Glume Blotch (Leptosphaeria nodorum; Bayer code LEPTNO)

Wheat plants (variety Yuma) were grown from seed in a greenhouse in 50% mineral soil/50% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Leptosphaeria nodorum 24 h after fungicide treatments. After inoculation the plants were kept in 100% relative humidity (one day in a dark dew chamber followed by two days in a lighted dew chamber at 20° C.) to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse set at 20° C. for disease to develop. Fungicide formulation, application and disease assessment followed the procedures as described in the Example A.

Example D: Evaluation of Fungicidal Activity: Apple Scab (Venturia inaequalis; Bayer Code VENTIN)

Apple seedlings (variety McIntosh) were grown in soil-less Metro mix, with one plant per pot. Seedlings with two expanding young leaves at the top (older leaves at bottom of the plants were trimmed) were used in the test. Plants were inoculated with a spore suspension of Venturia inaequalis 24 h after fungicide treatment and kept in a 22° C. dew chamber with 100% relative humidity for 48 h, and then moved to a greenhouse set at 20° C. for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

Example E: Evaluation of Fungicidal Activity: Leaf Spot of Sugar Beets (Cercospora beticola; Bayer Code CERCBE)

Sugar beet plants (variety HH88) were grown in soil-less Metro mix and trimmed regularly to maintain a uniform plant size prior to test. Plants were inoculated with a spore suspension 24 h after fungicide treatments. Inoculated plants were kept in a dew chamber at 22° C. for 48 h then incubated in a greenhouse set at 24° C. under a clear plastic hood with bottom ventilation until disease symptoms were fully expressed. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

Example F: Evaluation of Fungicidal Activity: Asian Soybean Rust (Phakopsora pachyrhizi; Bayer Code PHAKPA)

Technical grades of materials were dissolved in acetone, which were then mixed with nine volumes of H₂O containing 0.011% Tween 20. The fungicide solutions were applied onto soybean seedlings using an automated booth sprayer to run-off. All sprayed plants were allowed to air dry prior to further handling.

Soybean plants (variety Williams 82) were grown in soil-less Metro mix, with one plant per pot. Two weeks old seedlings were used for testing. Plants were inoculated either 3 days prior to or 1 day after fungicide treatments. Plants were incubated for 24 h in a dark dew room at 22° C. and 100% relative humidity then transferred to a growth room at 23° C. for disease to develop. Disease severity was assessed on the sprayed leaves.

Example G: Evaluation of Fungicidal Activity: Barley Scald (Rhyncosporium secalis Bayer Code RHYNSE)

Barley seedlings (variety Harrington) were propagated in soil-less Metro mix, with each pot having 8 to 12 plants, and used in the test when the first leaf was fully emerged. Test plants were inoculated by an aqueous spore suspension of Rhyncosporium secalis 24 h after fungicide treatments. After inoculation the plants were kept in a dew room at 22° C. with 100% relative humidity for 48 h. The plants were then transferred to a greenhouse set at 20° C. for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

Example H: Evaluation of Fungicidal Activity: Rice Blast (Pyricularia oryzae; Bayer Code PYRIOR)

Rice seedlings (variety Japonica) were propagated in soil-less Metro mix, with each pot having 8 to 14 plants, and used in the test when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension of Pyricularia oryzae 24 h after fungicide treatments. After inoculation the plants were kept in a dew room at 22° C. with 100% relative humidity for 48 h to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse set at 24° C. for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

Example I: Evaluation of Fungicidal Activity: Tomato Early Blight (Alternaria solani; Bayer Code ALTESO)

Tomato plants (variety Outdoor Girl) were propagated in soil-less Metro mix, with each pot having one plant, and used when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension of Alternaria solani 24 h after fungicide treatments. After inoculation the plants were kept in a dew room at 22° C. with 100% relative humidity for 48 h to permit spores to germinate and infect the leaf. The plants were then transferred to a growth room at 22° C. for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

Example J: Evaluation of Fungicidal Activity: Cucumber Anthracnose (Colletotrichum lagenarium; Bayer Code COLLLA)

Cucumber seedlings (variety Bush Pickle) were propagated in soil-less Metro mix, with each pot having one plant, and used in the test when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension of Colletotrichum lagenarium 24 hr after fungicide treatments. After inoculation the plants were kept in a dew room at 22° C. with 100% relative humidity for 48 hr to permit spores to germinate and infect the leaf. The plants were then transferred to a growth room set at 22° C. for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.

TABLE 1 Compound Structure, Preparation Method, and Appearance Prepared According- *Cmpd. To No. Structure Example Appearance 1

Example 1; Example 3A; Example 4A White Solid 2

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 3

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 4

Example 1; Example 2A; Example 3A; Example 4A Clear, Colorless Oil 5

Example 1; Example 2B; Example 3A; Example 4A Colorless Oil 6

Example 1; Example 2B; Example 3A; Example 4 A Colorless Oil 7

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 8

Example 1; Example 2C; Example 3A; Example 4A Colorless Oil 9

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 10

Example 1; Example 2 A; Example 3A; Example 4A Colorless Oil 11

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 12

Example 3E; Example 4A Colorless Oil 13

Example 3E; Example 4A Colorless Oil 14

Example 1; Example 3C; Example 4A Colorless Oil 15

Example 1; Example 3C; Example 4A Colorless Oil 16

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 18

Example 3F; Example 4A Colorless Oil 19

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 20

Example 1; Example 2A; Example 3A; Example 4A Clear Oil 21

Example 1; Example 2A; Example 3A; Example 4A Clear Oil 22

Example 1; Example 2A; Example 3A; Example 4A Clear Oil 23

Example 1; Example 2A; Example 3A; Example 4A Clear Oil 24

Example 1; Example 3C; Example 4A Sticky Wax 25

Example 1; Example 3C; Example 4A Sticky Wax 26

Example 1; Example 3C; Example 4A Sticky Wax 27

Example 1; Example 3C; Example 4A Sticky Wax 28

Example 1; Example 3C; Example 3D, Steps 1-2; Example 4A White Foam 29

Example 1; Example 3C; Example 3D, Steps 1-3; Example 4A Sticky Wax 31

Example 3F; Example 4A Clear Oil 33

Example 1; Example 3B; Example 4A White Solid 34

Example 1; Example 3B; Example 4A White Solid 35

Example 1; Example 2A; Example 3A; Example 4A White Solid 36

Example 1; Example 3B; Example 4A White Foam 37

Example 1; Example 2A; Example 3A; Example 4A Clear, Colorless Oil 38

Example 1; Example 2A; Example 3A; Example 4A Clear, Colorless Oil 39

Example 1; Example 2A; Example 3A; Example 4A Clear, Colorless Oil 40

Example 1; Example 2A; Example 3A; Example 4A White Foam 43

Example 1; Example 2A; Example 3A; Example 4A White Solid 44

Example 1; Example 2A; Example 3A; Example 4A White Solid 45

Example 5, Step 1 White Solid 46

Example 5, Step 1 Colorless Oil 47

Example 5, Step 1 Colorless Oil 48

Example 5, Step 1 Pale Yellow Oil 49

Example 5, Step 1 Colorless Oil 50

Example 5, Step 1 Colorless Oil 51

Example 5, Step 1 Colorless Oil 52

Example 5, Step 1 Colorless Oil 53

Example 5, Step 1 Colorless Oil 54

Example 5, Step 1 Colorless Oil 55

Example 5, Step 1 Colorless Oil 56

Example 5, Step 1 Colorless Oil 57

Example 5, Step 1 Colorless Oil 58

Example 5, Step 1 Colorless Oil 59

Example 5, Step 1 Colorless Oil 60

Example 5, Step 1 Colorless Oil 61

Example 5, Step 1 White Solid 63

Example 5, Step 1 Colorless Oil 64

Example 5, Step 1 Colorless Oil 65

Example 5, Step 1 Sticky Oil 66

Example 5, Step 1 Sticky Oil 67

Example 5, Step 1 Sticky Oil 68

Example 5, Step 1 Sticky Wax 69

Example 5, Step 1 Sticky Wax 70

Example 5, Step 1 Sticky Wax 71

Example 5, Step 1 White Solid 72

Example 5, Step 1 White Solid 73

Example 5, Step 1 White Solid 74

Example 5, Step 1 White Solid 75

Example 5, Step 1 White Solid 77

Example 5, Step 1 White Solid 78

Example 5, Step 1 White Solid 79

Example 5, Step 1 White Solid 80

Example 1; Example 3B; Example 4A; Example 5, Step 1 Sticky Oil 81

Example 5, Step 1 Sticky Oil 83

Example 5, Step 1 Colorless Oil 84

Example 5, Step 1 Clear, Colorless Oil 85

Example 5, Step 1 Clear, Colorless Oil 86

Example 5, Step 1 White Solid 87

Example 5, Step 1 White Solid 88

Example 5, Step 1 White Solid 89

Example 5, Step 2 White Solid 90

Example 5, Step 2 White Foam 91

Example 5, Step 2 Colorless Oil 92

Example 5, Step 2 White Foam 93

Example 5, Step 2 White Foam 95

Example 5, Step 2 Colorless Oil 96

Example 5, Step 2 White Foam 97

Example 5, Step 2 Colorless Oil 98

Example 5, Step 2 Colorless Oil 99

Example 5, Step 2 Colorless Oil 100

Example 5, Step 2 Colorless Oil 101

Example 5, Step 2 Colorless Oil 102

Example 5, Step 2 Colorless Oil 103

Example 5, Step 2 Colorless Oil 104

Example 5, Step 2 Colorless Oil 105

Example 5, Step 2 Colorless Oil 106

Example 5, Step 2 Colorless Gel 107

Example 5, Step 2 Colorless Gel 109

Example 5, Step 2 Colorless Oil 110

Example 5, Step 2 Clear, Colorless Oil 111

Example 5, Step 2 Clear, Colorless Oil 112

Example 5, Step 2 Clear, Colorless Oil 113

Example 5, Step 2 White Solid 114

Example 5, Step 2 White Solid 115

Example 5, Step 2 White Solid 116

Example 5, Step 2 White Solid 117

Example 5, Step 2 White Foam 118

Example 5, Step 2 White Foam 119

Example 5, Step 2 White Foam 120

Example 5, Step 2 White Foam 121

Example 5, Step 2 White Foam 122

Example 5, Step 2 White Foam 123

Example 5, Step 2 White Foam 124

Example 5, Step 2 White Foam 125

Example 5, Step 2 White Solid 127

Example 5, Step 2 White Solid 128

Example 5, Step 2 White Solid 129

Example 5, Step 2 White Solid 130

Example 5, Step 2 Clear, Colorless Oil 131

Example 5, Step 2 Clear, Colorless Oil 132

Example 5, Step 2 Colorless Foam 133

Example 5, Step 2 Colorless Foam 135

Example 5, Step 2 Colorless Tacky Semi- Solid 136

Example 5, Step 2 White Foam 137

Example 5, Step 2 White Foam 138

Example 6B Colorless Semi-Solid 139

Example 6A Colorless Oil 140

Example 6A White Foam 141

Example 6B White Foam 142

Example 6C White Foam 143

Example 6A Colorless Oil 144

Example 6B Colorless Oil 145

Example 6A Colorless Oil 146

Example 6B Colorless Oil 147

Example 6B Colorless Oil 148

Example 6B Colorless Oil 149

Example 6B Colorless Oil 150

Example 6A Colorless Oil 152

Example 6A Colorless Oil 153

Example 6B Colorless Oil 155

Example 6A Colorless Oil 156

Example 6A Colorless Oil 157

Example 6A Colorless Oil 158

Example 6B Colorless Oil 159

Example 6B Colorless Oil 160

Example 6B Colorless Oil 161

Example 6A Colorless Oil 162

Example 6A Colorless Oil 163

Example 6B Colorless Oil 164

Example 6B Colorless Oil 165

Example 6A Colorless Oil 166

Example 6A Colorless Oil 167

Example 6A Colorless Oil 168

Example 6A Colorless Oil 169

Example 6B Colorless Oil 170

Example 6B Colorless Oil 171

Example 6B Colorless Oil 173

Example 6A Colorless Oil 174

Example 6A Colorless Oil 175

Example 6B Colorless Oil 176

Example 6B Colorless Oil 178

Example 6B Clear, Colorless Oil 179

Example 6B Clear, Colorless Oil 180

Example 6B Clear, Colorless Oil 181

Example 6B White Foam 182

Example 6A Colorless Oil 183

Example 6B White Solid 184

Example 6B White Solid 185

Example 6B White Solid 186

Example 6B White Solid 187

Example 6A White Solid 188

Example 6A White Solid 189

Example 6A White Solid 190

Example 6A White Solid 191

Example 6B White Solid 192

Example 6B While Foam 193

Example 6B Sticky Wax 194

Example 6B White Foam 195

Example 6B White Foam 196

Example 6B White Foam 197

Example 6B White Foam 198

Example 6B Sticky Wax 199

Example 6B White Solid 201

Example 6B White Solid 202

Example 6B White Solid 203

Example 6B White Solid 204

Example 6A White Solid 206

Example 6A White Solid 207

Example 6A White Solid 208

Example 6A Clear Colorless Oil 209

Example 6A Slightly Cloudy Colorless Oil 210

Example 6A Slightly Cloudy Colorless Oil 211

Example 6C Clear Colorless Oil 212

Example 6C Colorless Clear Film And Opaque Oil 213

Example 6A Clear Colorless Viscous Oil And Semi- Solid 214

Example 6B Clear, Colorless Oil 215

Example 6A Pale Yellow Oil 216

Example 6A Pale Yellow Oil 217

Example 6A Pale Yellow Oil 218

Example 6B Pale Yellow Oil 219

Example 6B Pale Yellow Oil 220

Example 6B Pale Yellow Oil 221

Example 6B While Foam 222

Example 6B While Foam 223

Example 6A While Foam 224

Example 6A While Foam 225

Example 6B Slightly Opaque Colorless Oil 226

Example 1; Example 2D, Steps 1- 2; Example 3A; Example 4A While Semi- Solid 227

Example 5, Step 1 White Glass 228

Example 5, Step 2 Colorless Foam 229

Example 6A Clear, Colorless Oil 230

Example 6B Clear, Colorless Oil 232

Example 5, Step 1 White Semi- Solid 233

Example 1; Example 2A; Example 3A; Example 4A Clear, Colorless Viscous Oil 234

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 235

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 236

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 237

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 238

Example 1; Example 2A; Example 3A; Example 4A. Slightly Cloudy Colorless Viscous Oil 239

Example 1; Example 2A; Example 3A; Example 4A. Slightly Cloudy Colorless Viscous Oil 240

Example 1; Example 2A; Example 3A; Example 4A. White Foam 241

Example 3H Steps 1-2; Example 4A. Colorless Oil 242

Example 3G, Steps 1 and 2; Example 4A Colorless Oil 243

Example 3G, Steps 1 and 2; Example 4A Colorless Oil 244

Example 4A Colorless Oil 245

Example 1; Example 3C; Exasnple 4A. White Foam 246

Example 1; Example 2A; Example 3A; Example 4A. White Foam 247

Example 1; Example 3C; Example 4A. White Foam 248

Example 1; Example 2A; Example 3A; Example 4A. White Foam 249

Example 3G, Steps 1 and 2; Example 4A White Foam 250

Example 1; Example 2A; Example 3A; Example 4A. White Semisolid 251

Example 1; Example 2A; Example 3A; Example 4A. White Semisolid 252

Example 1; Example 2A; Example 3A; Example 4A. White Semisolid 253

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 254

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 255

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 256

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 257

Example 1; Example 2A; Example 3A; Example 4A. Clear, Colorless Oil 258

Example 3I; Example 4A White Foam 259

Example 1; Example 2A; Example 3A; Example 4A. White Foam 260

Example 1; Example 2A; Example 3A; Example 4A. Colorless Oil 261

Example 1; Example 2A; Example 3A; Example 4A. Colorless Oil 262

Example 1; Example 2A; Example 3A; Example 4A. Colorless Oil 263

Example 1; Example 2A; Example 3A; Example 4A. Colorless Oil 264

Example 1; Example 2A; Example 3A; Example 4A. White Foam 265

Example 1; Example 2A: Example 3A; Example 4A. Colorless Oil 266

Example 1; Example 2A; Example 3A; Example 4A. Sticky Wax 267

Example 1; Example 2A; Example 3A; Example 4A. Sticky Wax. 268

Example 3I, Example 4A Oil 269

Example 3I, Example 4A Oil 270

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 271

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 272

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 273

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 274

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 275

Example 3F; Example 4A Colorless Oil 276

Example 3F; Example 4A Colorless Oil 277

Example 3F; Example 4A Colorless Oil 278

Example 3F; Example 4A Colorless Oil 279

Example 3F; Example 4A Colorless Oil 280

Example 3F; Example 4A Colorless Oil 281

Example 3F; Example 4A Colorless Oil 282

Example 3F; Example 4A Colorless Oil 283

Example 3F; Example 4A Colorless Oil 284

Example 3F; Example 4A Colorless Oil 285

Example 3F; Example 4A Colorless Oil 286

Example 3F; Example 4A Colorless Oil 287

Example 3F; Example 4A Colorless Oil 288

Example 3F; Example 4A White Foam 289

Example 3F; Example 4A Yellow Sticky Wax 290

Example 3F; Example 4A White Foam 291

Example 3F; Example 4A Yellow Sticky Wax 292

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 293

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 294

Example 1; Example 2A; Example 3A; Example 4A Colorless Oil 295

Example 3F; Example 4A Colorless Oil 296

Example 3F; Example 4A Colorless Oil 297

Example 3F; Example 4A Colorless Oil 298

Example 3F; Example 4A Colorless Oil 299

Example 3F; Example 4A Colorless Oil 300

Example 3F; Example 4A Colorless Oil 301

Example 3F; Example 4A Colorless Oil 302

Example 3F; Example 4A Colorless Oil 303

Example 3F; Example 4A Colorless Oil 304

Example 3F; Example 4A Colorless Oil 305

Example 3F; Example 4A Colorless Oil 306

Example 3F; Example 4A Colorless Oil 307

Example 3F; Example 4A Colorless Oil 308

Example 3F; Example 4A Thick Oil 309

Example 3F; Example 4A Colorless Oil 310

Example 5, Step 1. White Powder 311

Example 5, Step 1. White Powder 312

Example 5, Step 1. Clear, Colorless Thick Oil 313

Example 5, Step 1. White Powder 314

Example 5, Step 1. White Semi- Solid 315

Example 5, Step 1. White Semi- Solid 316

Example 5, Step 1. Clear Glass 317

Example 1; Example 2A; Example 3A; Example 4A. Example 5, step 1. Pale Purple Sticky Wax 318

Example 5 Step 1. Colorless Oil 319

Example 5, Step 1 White Foam 320

Example 5, Step 1 White Foam 321

Example 5, Step 1 White Solid 322

Example 5, Step 1. Colorless Oil 323

Example 5, Step 1. Yellow Oil 324

Example 5, Step 1. Yellow Oil 325

Example 5, Step 1. Yellow Oil 326

Example 5, Step 1. Yellow Oil 327

Example 5, Step 1 White Foam 328

Example 5, Step 1 White Foam 329

Example 5, Step 1 White Foam 330

Example 5, Step 1 White Foam 331

Example 5, Step 1 White Foam 332

Example 5, Step 1 Clear, Colorless Oil 333

Example 5, Step 1. Light Brown Oil 334

Example 5, Step 1. Pale Yellow Oil 335

Example 5, Step 1. Pale Yellow Oil 336

Example 5, Step 1. White Powdery Solid 337

Example 5, Step 1. Clear, Colorless Oil 338

Example 5, Step 1. Whitc Powdery Solid 339

Example 5, Step 1. Clear, Colorless Oil 340

Example 5, Step 1. Whitc Solid 341

Example 5, Step 1. Thick Oil 342

Example 5, Step 1. White Solid 343

Example 5, Step 1. White Solid 344

Example 5, Step 1. White Solid 345

Example 5, Step 1. White Solid 346

Example 5, Step 1. Thick Oil 347

Example 5, Step 1. White Solid 348

Example 5, Step 1. White Solid 349

Example 5, Step 1 Oil 350

Example 5, Step 1 Oil 351

Example 5, Step 1 Oil 352

Example 5, Step 1 Colorless Oil 353

Example 5, Step 1 Colorless Oil 354

Example 5, Step 1 Colorless Oil 355

Example 5, Step 1 Colorless Oil 356

Example 5, Step 1 Colorless Oil 357

Example 5, Step 1 Colorless Oil 358

Example 5, Step 1 Colorless Oil 359

Example 5, Step 1 Colorless Oil 360

Example 5, Step 1 Colorless Oil 361

Example 5, Step 1 Colorless Foam 362

Example 5, Step 1 Colorless Foam 363

Example 5, Step 1 Colorless Oil 364

Example 5, Step 1 Colorless Oil 365

Example 5, Step 1 White Foam 366

Example 5, Step 1. Sticky Wax 367

Example 5, Step 1. Sticky Wax 368

Example 5, Step 1. Sticky Wax 369

Example 5, Step 1. Sticky Wax 370

Example 5, Step 1. White Foam 371

Example 5, Step 1 White Foam 372

Example 5, Step 1 White Foam 373

Example 5, Step 1 White Foam 374

Example 5, Step 1 White Foam 375

Example 5, Step 1 Colorless Oil 376

Example 5, Step 1 Colorless Oil 377

Example 5, Step 1. Thick Oil 378

Example 5, Step 1. Thick Oil 379

Example 5, Step 1. White Solid 380

Example 5, Step 1. Thick Oil 381

Example 5, Step 1. Thick Oil 382

Example 5, Step 1. White Foam 383

Example 5, Step 1. White Solid 384

Example 5, Step 1. White Foam 385

Example 5, Step 1. White Foam 386

Example 5 Step 2. Matte White Solid And Clear Oil 387

Example 5 Step 2. Matte White Solid And Clear Oil 388

Example 5, Step 2. Clear, Colorless Oil 389

Example 5, Step 2. Colorless Foam 390

Example 5, Step 2. Colorless Foam 391

Example 5, Step 2. Clear, Colorless Oil 392

Example 5, Step 2. Semi Solid 393

Example 5, Step 2. White Foam 394

Example 5 Step 2. Colorless Foamy Oil 395

Example 5, Step 2. White Foam 396

Example 5, Step 2 White Foam 397

Example 5, Step 2 White Foam 398

Example 5, Step 2 White Foam 399

Example 5, Step 2. White Foam 400

Example 5, Step 2. White Foam 401

Example 5, Step 2. White Foam 402

Example 5, Step 2. White Foam 403

Example 5, Step 2 Colorless Oil 404

Example 5, Step 2 Colorless Oil 405

Example 5, Step 2 White Foam 406

Example 5, Step 2 White Foam 407

Example 5, Step 2 White Foam 408

Example 5, Step 2 White Foam 409

Example 5, Step 2 White Foam 410

Example 5, Step 2 White Foam 411

Example 5, Step 2 White Foam 412

Example 5, Step 2 Oil 413

Example 5, Step 2 White Foam 414

Example 5, Step 2. Thick Oil 415

Example 5, Step 2. White Foam 416

Example 5, Step 2. White Foam 417

Example 5, Step 2. White Foam 418

Example 5, Step 2. White Foam 419

Example 5, Step 2. White Foam 420

Example 5, Step 2. Colorless Foam 421

Example 5, Step 2. Clear, Colorless Oil 422

Example 5, Step 2. Clear, Colorless Oil 423

Example 5, Step 2. Colorless Foam 424

Example 5, Step 2. Colorless Foam 425

Example 5, Step 2. Clear, Colorless Oil 426

Example 5, Step 2. Clear, Colorless Oil 427

Example 5, Step 2. Clear, Colorless Oil 428

Example 5, Step 2. White Foam 429

Example 5, Step 2. Sticky Wax 430

Example 5, Step 2 Colorless Gel 431

Example 5, Step 2 Colorless Gel 432

Example 5, Step 2 Colorless Gel 433

Example 5, Step 2 Colorless Gel 434

Example 5, Step 2 Colorless Oil 435

Example 5, Step 2 Colorless Oil 436

Example 5, Step 2 Colorless Oil 437

Example 5, Step 2 Colorless Oil 438

Example 5, Step 2 Colorless Foam 439

Example 5, Step 2 Colorless Foam 440

Example 5, Step 2 Colorless Oil 441

Example 5, Step 2 Colorless Oil 442

Example 5, Step 2 White Foam 443

Example 5, Step 2. White Foam 444

Example 5, Step 2. White Foam 445

Example 5, Step 2. White Foam 446

Example 5, Step 2. White Foam 447

Example 5, Step 2 White Foam 448

Example 5, Step 2 White Foam 449

Example 5, Step 2 White Foam 450

Example 5, Step 2 White Foam 451

Example 5, Step 2 White Foam 452

Example 5, Step 2 Colorless Oil 453

Example 5, Step 2 Colorless Oil 454

Example 5, Step 2. White Foam 455

Example 5, Step 2. White Foam 456

Example 5, Step 2. White Foam 457

Example 5, Step 2. White Foam 458

Example 5, Step 2. White Foam 459

Example 5, Step 2. White Foam 460

Example 5, Step 2. White Foam 461

Example 5, Step 2. White Foam 462

Example 6B. Slightly Opaque Colorless Viscous Oil 463

Example 6B. White Foam Slightly Opaque Colorless Viscous Oil 464

Example 6B. Yellow Oil 465

Example 6B. Clear, Colorless Oil 466

Example 6B. Pale Yellow Oil 467

Example 6B. Pale Yellow Oil 468

Example 6A. Fluffy White Powder 469

Example 6A. Clear, Colorless Oil 470

Example 6A. Clear, Colorless Oil 471

Example 6A. Clear, Colorless Oil 472

Example 6B. White Foam 473

Example 6B. Sticky Wax 474

Example 6B. Colorless Oil 475

Example 6A. White Foam 476

Example 6B. White Foam 477

Example 6A. White Foam 478

Example 6A. White Foam 479

Example 6A. White Foam 480

Example 6B. White Foam 481

Example 6B. White Foam 482

Example 6B. White Foam 483

Example 6B. White Foam 484

Example 6B. White Foam 485

Example 6A Colorless Oil 486

Example 6A Colorless Oil 487

Example 6B Colorless Oil 488

Example 6A. White Foam 489

Example 6A. White Foam 490

Example 6A. White Wax 491

Example 6A. White Foam 492

Example 6A. White Foam 493

Example 6B White Foam 494

Example 6C White Foam 495

Example 6A White Foam 496

Example 6A White Foam 497

Example 6A Colorless Film 498

Example 6A. White Foam 499

Example 6A. White Foam 500

Example 6A. White Foam 501

Example 6A. White Foam 502

Example 6A. White Foam 503

Example 6A. White Foam 504

Example 6A. White Foam 505

Example 6A. Clear, Colorless Oil 506

Example 6A. Clear, Colorless Oil 507

Example 6A. Clear, Colorless Oil 508

Example 6A. Clear, Colorless Oil 509

Example 6A. Clear, Colorless Oil 510

Example 6A. Clear, Colorless Oil 511

Example 6A. Clear, Colorless Oil 512

Example 6A. Clear, Colorless Oil 513

Example 6B. Clear, Colorless Oil 514

Example 6B. Clear, Colorless Oil 515

Example 6B. Clear, Colorless Oil 516

Example 6B. Clear, Colorless Oil 517

Example 6B. Clear, Colorless Oil 518

Example 6B. Clear, Colorless Oil 519

Example 6B. Clear, Colorless Oil 520

Example 6B. Clear, Colorless Oil 521

Example 6A. White Foam 522

Example 6A. Sticky White Foam 523

Example 6A Colorless Oil 524

Example 6A Colorless Oil 525

Example 6A Colorless Oil 526

Example 6A Colorless Oil 527

Example 6A Colorless Foam 528

Example 6A Colorless Foam 529

Example 6A Colorless Foam 530

Example 6A Colorless Foam 531

Example 6A Colorless Oil 532

Example 6A Colorless Oil 533

Example 6A Colorless Oil 534

Example 6A Colorless Oil 535

Example 6A. White Foam 536

Example 6A. White Foam 537

Example 6A. White Foam 538

Example 6A. White Foam 539

Example 6A. White Foam 540

Example 6A. White Foam 541

Example 6A. White Foam 542

Example 6A. White Foam 543

Example 6A. White Foam 544

Example 6A. White Foam 545

Example 6A. White Foam 546

Example 6A. White Foam 547

Example 6A. White Foam 548

Example 6A. White Foam 549

Example 6A. White Foam 550

Example 6A. White Foam 551

Example 6A. White Foam 552

Example 6A. White Foam 553

Example 6A Colorless Foam 554

Example 6A Colorless Foam *Cmpd. No. — Compound Number

Lengthy table referenced here US10588318-20200317-T00001 Please refer to the end of the specification for access instructions.

Lengthy table referenced here US10588318-20200317-T00002 Please refer to the end of the specification for access instructions.

Lengthy table referenced here US10588318-20200317-T00003 Please refer to the end of the specification for access instructions.

Lengthy table referenced here US10588318-20200317-T00004 Please refer to the end of the specification for access instructions.

Lengthy table referenced here US10588318-20200317-T00005 Please refer to the end of the specification for access instructions.

Lengthy table referenced here US10588318-20200317-T00006 Please refer to the end of the specification for access instructions.

LENGTHY TABLES The patent contains a lengthy table section. A copy of the table is available in electronic form from the USPTO web site (http://seqdata.uspto.gov/?pageRequest=docDetail&DocID=US10588318B2). An electronic copy of the table will also be available from the USPTO upon request and payment of the fee set forth in 37 CFR 1.19(b)(3). 

What is claimed is:
 1. A compound of Formula I

wherein: X is hydrogen or C(O)R₅; Y is hydrogen, C(O)R₅, or Q; Q is

wherein: Z is N or CH; R₁ is hydrogen or alkyl, substituted with 0, 1 or multiple R₈; R₂ is methyl; R₃ is chosen from aryl or heteroaryl, each substituted with 0, 1 or multiple R₈; R₄ is chosen from hydrogen, halo, hydroxyl, alkyl or alkoxy; R₅ is chosen from alkoxy or benzyloxy, each substituted with 0, 1, or multiple R₈; R₆ is chosen from hydrogen, alkoxy, or halo, each substituted with 0, 1, or multiple R₈; R₇ is chosen from hydrogen, —C(O)R₉, or —CH₂OC(O)R₉; R₈ is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, alkynyl, alkoxy, cyano or heterocyclyl, each substituted with 0, 1, or multiple R₁₀; R₉ is chosen from alkyl, alkoxy, or aryl, each optionally substituted with 0, 1, or multiple R₈; R₁₀ is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, alkoxy, or heterocyclyl; R₁₁ is chosen from hydrogen or alkyl, substituted with 0, 1 or multiple R₈; and R₁₂ is chosen from aryl or heteroaryl, each substituted with 0, 1 or multiple R₈.
 2. The compound according to claim 1, wherein X and Y are hydrogen.
 3. The compound according to claim 2, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl.
 4. The compound according to claim 2, wherein R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈.
 5. The compound according to claim 2, wherein R₄ is H.
 6. The compound according to claim 2, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl, R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈, and R₄ is H.
 7. The compound according to claim 1, wherein X is C(O)R₅ and Y is hydrogen.
 8. The compound according to claim 7, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl.
 9. The compound according to claim 7, wherein R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈.
 10. The compound according to claim 7, wherein R₄ is H.
 11. The compound according to claim 7, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl, R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈, and R₄ is H.
 12. The compound according to claim 1, wherein X is hydrogen and Y is Q.
 13. The compound according to claim 12, wherein Z is N.
 14. The compound according to claim 13, wherein R₆ is alkoxy.
 15. The compound according to claim 14, wherein R₇ is hydrogen.
 16. The compound according to claim 15, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl.
 17. The compound according to claim 15, wherein R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈.
 18. The compound according to claim 15, wherein R₄ is H.
 19. The compound according to claim 15, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl, R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈, and R₄ is H.
 20. The compound according to claim 14, wherein R₇ is chosen from —C(O)R₉, or —CH₂OC(O)R₉.
 21. The compound according to claim 20, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl.
 22. The compound according to claim 20, wherein R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈.
 23. The compound according to claim 20, wherein R₄ is H.
 24. The compound according to claim 20, wherein R₁ and R₁₁ are independently chosen from hydrogen or alkyl, R₃ and R₁₂ are independently aryl, each substituted with 0, 1 or multiple R₈, and R₄ is H.
 25. The compound according to claim 24, wherein R₉ is chosen from —CH₃, +CH₂OCH₂CH₃, —CH₂CH₂OCH₃, —CH(CH₃)₂, —CH₂CH₂CH₂CH₃, or -cyclopropyl.
 26. A composition for the control of a fungal pathogen including mixtures of at least one of the compounds of claim 1 and another pesticide selected from the group consisting of fungicides, insecticides, nematocides, miticides, arthropodicides, bactericides and combinations thereof.
 27. A composition for the control of a fungal pathogen including mixtures of at least one of the compounds of claim 15 and another pesticide selected from the group consisting of fungicides, insecticides, nematocides, miticides, arthropodicides, bactericides and combinations thereof.
 28. A composition for the control of a fungal pathogen including mixtures of at least one of the compounds of claim 20 and another pesticide selected from the group consisting of fungicides, insecticides, nematocides, miticides, arthropodicides, bactericides and combinations thereof.
 29. A method for the control of fungal attack on a plant, the method including the step of: applying a fungicidally effective amount of at least one of the compounds of claim 1 to at least one of the plant, an area adjacent to the plant, soil adapted to support growth of the plant, a root of the plant, and foliage of the plant.
 30. A method for the control of fungal attack on a plant, the method including the step of: applying a fungicidally effective amount of at least one of the compositions of claim 26 to at least one of the plant, an area adjacent to the plant, soil adapted to support growth of the plant, a root of the plant, and foliage of the plant. 